Marder Group


    The latest publications


    381. Y.P. Budiman, S.A. Westcott, U. Radius, and T.B. Marder, “Fluorinated Aryl Boronates as Building Blocks in Organic                                       Synthesis,” Adv. Synth. Catal. xx: xxxx-xxxx (202x). DOI: 10.1002/adsc.202001291. (Accepted Article, November 2020). Invited          review for special thematic issue on Boron in Catalysis and Organic Synthesis (E. Fernandez, Guest Editor).               

             (Designated as a Very Important Paper).

    380. J. He, F. Rauch, I. Krummenacher, H. Braunschweig, M. Finze, and T.B. Marder, “Two Derivatives of Phenylpyridyl-                                         fused Boroles with Contrasting Electronic Properties: Decreasing and Enhancing the Electron Accepting Ability,” Dalton Trans.           xx: xxxx-xxxx (202x). DOI: 10.1039/D0DT03619F.

    379. J. He, F. Rauch, A. Friedrich, J. Krebs, I. Krummenacher, R. Bertermann, J. Nitsch, H. Braunschweig, M. Finze,                                               and T.B. Marder, “Phenylpyridyl-fused Boroles: A Unique Coordination Mode and Weak B–N Coordination-Induced                                       Dual Fluorescence,” Angew. Chem. Int. Ed., xx: xxxx-xxxx (202x). DOI: 10.1002/anie.202013692; Angew. Chem., 13x: xxxx-                         xxxx (202x). DOI: 10.1002/ange.202013692 (Accepted Article, November 2020).

    378. G.K. Kole, J. Merz, A. Amar, B. Fontaine, A. Boucekkine,J. Nitsch, S. Lorenzen, A- Friedrich, I. Krummenacher,                                           M. Košćak, H. Braunschweig, I. Piantanida, J.-F. Halet, K. Müller-Buschbaum, and T.B. Marder, “2- and 2,7-                                                     Substituted para-N-Methylpyridinium Pyrenes: Syntheses, Molecular and Electronic Structures, Photophysical,                                             Electrochemical, and Spectroelectrochemical Properties and Binding to Double Stranded (ds)-DNA,” Chem. Eur. J.,                                 2x: xxx-xxx (202x). DOI: 10.1002/chem.202004648. (Accepted Article, November 2020). DOI: 10.1002/chem.202004748.

    377.  J. He, F. Rauch, M. Finze, and T.B. Marder, “(Hetero)Arene-Fused Boroles: A Broad Spectrum of Applications,” Chem.                                 Sci., 11: xxxx-xxxx (2020). DOI: 10.1039/d0sc05676f. (Accepted Article, November 2020).

    376. Y.P. Budiman, S. Lorenzen, Z. Liu, U. Radius, and T.B. Marder, “Base-Free Pd-catalyzed C-Cl Borylation of Fluorinated Aryl  
             Chlorides,” Chem. Eur. J., 2x: xxx-xxx (202x). DOI: 10.1002/chem.202004648. (Accepted Article, November 2020).

    375. A. Friedrich, I.E. Collings, K.F. Dziubek, S. Fanetti, K. Radacki, J. Ruiz-Fuertes, J. Pellicer-Porres, M. Hanfland,                                                 D. Sieh, R. Bini, S.J. Clark, and T.B. Marder, “Pressure-Induced Polymerization of Polycyclic Arene-Perfluoroarene Cocrystals:                    Single Crystal X-ray Diffraction Studies, Reaction Kinetics, and Design of Columnar Hydrofluorocarbons,” J. Am. Chem. Soc., 142:          18907-18923 (2020). DOI: 10.1021/jacs.0c09021. Read more...

             JACS Spotlight: J. Am. Chem. Soc., 142: 18733-18734 (2020). DOI: 10.1021/jacs.0c11191. Read more...

    374. M.W. Kuntze-Fechner, H. Verplancke, L. Tendera, M. Diefenbach, I. Krummenacher, H. Braunschweig,                                                               T.B. Marder, M.C. Holthausen, and U. Radius, “Coligand Role in the NHC Nickel catalyzed C–F Bond Activation: Investigations on          the Insertion of bis(NHC) Nickel into the C–F Bond of Hexafluorobenzene,” Chem. Sci., 11: 11009-11023 (2020). DOI:                                10.1039/D0SC04237D. Read more...

    373. Y.M. Tian, X.N. Guo, I. Krummenacher, Z. Wu, J. Nitsch, H. Braunschweig, U. Radius, and T.B. Marder,                                                              “Visible-Light-Induced Ni-Catalyzed Radical Borylation of Chloroarenes,”  J. Am. Chem. Soc., 142: 18231–18242 (2020).                             DOI: 10.1021/jacs.0c08834. Read more...

    372. X. Ma, J. Maier, M. Wenzel, A. Friedrich, A. Steffen, T.B. Marder, R. Mitrić and T. Brixner, “Direct observation of                                              o-benzyne formation in photochemical hexadehydro-Diels–Alder (hn-HDDA) reactions,” Chem. Sci., 11: 9198-9208 (2020).                       DOI: 10.1039/D0SC03184D. Read more...

    371. U. Müller, L. Roos, M. Frank, M. Deutsch, S. Hammer, M. Krumrein, A. Friedrich, T.B. Marder, B. Engels, A. Krueger,                                       and J. Pflaum, “Role of Intermolecular Interactions in the Excited Stare Photophysics of Tetracene and “2,2’-Ditetracene,”                          J. Phys. Chem., Part C, 124: 19435-19446 (2020). DOI: 10.11021/acs.jpc.0c04066.

    370. F.-P. Wu, X. Luo, U. Radius, T.B. Marder, and X.-F. Wu, “Copper-Catalyzed Synthesis of Stereodefined Cyclopropyl                                         Bis(Boronates) from Alkenes with CO as the C1 Source,” J. Am. Chem. Soc., 142: 14074-14079 (2020). DOI:                                                 10.1021/jacs.0c06800. Read more...

    369. Z. Liu, Y.P. Budiman, Y.-M. Tian, A. Friedrich, M. Huang, S.A. Westcott, U. Radius, and T.B. Marder, “Copper-Catalyzed                                     Oxidative Cross-Coupling of Electron-Deficient Polyfluorophenylboronate Esters with Terminal Alkynes,” Chem. Eur. J.,                               XXX (2020). DOI: 10.1002/chem.202002888. Read more...

    368. J. Maier, M. Deutsch,  J. Merz, Q. Ye, O. Diamond, M.T.  Schilling, A. Friedrich, B. Engels, and T.B. Marder, “Highly                                     Conjugated π-Systems Arising from Cannibalistic Hexadehydro-Diels-Alder Couplings: Cleavage of C‒C Single and Triple                           Bonds,” Chem. Eur. J., 26: XXX (2020). DOI: 10.1002/chem.202002511. Read more...

    367. Y.-M. Tian, X.-N. Guo, Zhu Wu, A. Friedrich, S.A. Westcott, H. Braunschweig, U. Radius, and T.B. Marder, “Ni-catalyzed                           traceless, directed C3 selective C-H borylation of indoles,” J. Am. Chem. Soc., 142: 13136-13144 (2020).                                                       DOI: 10.1021/jacs.0c05434. Read more...

    366. Z.-F. Jiao, Y.-M. Tian, B. Zhang, C.-H. Hao, Y. Qiao, Y.-X. Wang, Y. Qin, U. Radius, H.Braunschweig, T.B. Marder, X.-N. Guo                               X.-Y. Guo, “High Photocatalytic Activity of a NiO Nanodot-decorated Pd/SiC Catalyst for the Suzuki-Miyaura Cross-coupling of Aryl          Bromides and Chlorides in Air under Visible Light,” J. Catal., 389: 517-524 (2020). DOI: 10.1016/j.jcat.2020.06.025.                                     Read more... 

    365. Z. Wu, J. Nitsch, J. Schuster, A. Friedrich, K. Edkins, M. Loebnitz, F. Dinkelbach, V. Stepanenko, F.Würthner, C.M. Marian,                              L. Ji, and T.B. Marder “Persistent room temperature phosphorescence from triarylboranes,” Angew. Chem. Int. Ed.,                                     59: 17137-17144 (2020). DOI: 10.1002/anie.202007610; Angew. Chem., 132: 17285-17292 (2020).                                                                 DOI: 10.1002/ange.202007610 Read more...  

             (Designated as a Very Important Paper).

    364. H.-C. Schmitt, I. Fischer, L. Ji, J. Merz, T.B. Marder, J. Hoche, M.I.S. Röhr, and R. Mitric, “Isolated 2-Hydroxypyrene and                             its Dimer: A Frequency- and Time-Resolved Spectroscopic Study,” New J. Chem., xxx (2020). DOI: 10.1039/d0nj02391d.                            Read more...

    363. F. Rauch, J. Krebs, J. Günther, A. Friedrich, M. Hähnel, I. Krummenacher, H. Braunschweig, M. Finze, and T.B. Marder,                            “Electronically-driven Regioselective Iridium-catalyzed C−H Borylation of Donor-π-acceptor Chromophores Containing Triarylboron          Acceptors,” Chem. Eur. J., 26: 10626-10633 (2020). DOI: 10.1002/chem.202002348. Read more...

    362. F. Rauch, P. Endres, A. Friedrich, D. Sieh, M. Haehnel, I. Krummenacher, H. Braunschweig, M. Finze, L. Ji, and T.B. Marder,                            “An Iterative Divergent Approach to Conjugated Starburst Borane Dendrimers,” Chem. Eur. J., 26: 12951-129633 (2020).                             DOI: 10.1002/chem.202001985.  Read more...

             (Designated as a Hot Paper).

    361. J. Merz, L. Dietrich, J. Nitsch, I. Krummenacher, H. Braunschweig, M. Moos, D. Mims, C. Lambert, and T.B. Marder,                                     “Synthesis, Photophysical and Electronic Properties of Mono-, Di-, Tri-Amino-Substituted Ortho-Perylenes, and Comparison to the          Tetra-Substituted Derivative,” Chem. Eur. J., 26: 12050-12059 (2020). DOI: 10.1002/chem.202001475.                                                          Read more...

    360. J. Kubicki, M. Lorenc, P. Cochelin, O. Mongin, A. Amar, A. Boucekkine, A. Gaje,  M.G. Humphrey, M. Morshedi, S. Lorenzen,                          F. Rauch, C. Scheufler, T.B. Marder, and F. Paul, “Nitro End-Groups: Remarkable Vibrational Reporters for Charge Transfer in the               Excited States of Oligo(p-Phenyleneethynylene)-Bridged Donor-Acceptor Dyads," J. Phys. Chem. C, 124: 9755−9764 (2020).                      DOI: 10.1021/acs.jpcc.0c01532. Read more...

    359. A.K. Narsaria, F. Rauch, J. Krebs, P. Endres, A. Friedrich, I. Krummenacher, H. Braunschweig, M. Finze, J. Nitsch,                                          F.M. Bickelhaupt, and T.B. Marder, “Computationally Guided Molecular Design to Minimize the LE/CT Gap in D-π-A Fluorinated                Triarylboranes for Efficient TADF via D and π-Bridge Tuning,” Adv. Funct. Mater., 30: 2002064 (2020). (15 pages)                                          DOI: 10.1002/adfm.202002064. Read more...             

    358. M.J. Krahfuß, J. Nitsch, F.M. Bickelhaupt, T.B. Marder, and Udo Radius, “N-Heterocyclic Silylenes as Ligands in Transition Metal               Carbonyl Chemistry: Nature of their Bonding and Supposed Innocence,” Chem. Eur. J., 26: 11276-11292 (2020).                                          DOI: 10.1002/chem.202001062. Read more...

    357. L. Kuehn, A.F. Eichhorn, D. Schmidt, T.B. Marder, and U. Radius, “NHC-stabilized Copper(I) Aryl Complexes and their                                    Transmetalation Reaction with Aryl Halides,” invited paper for F. Ekkehardt Han 60th birthday issue, J. Organomet. Chem., 919:                121249 (2020). DOI: 10.1016/j.jorganchem.2020.121249. Read more...

    356. Y.P. Budiman, A. Jayaraman, A. Friedrich, F. Kerner, U. Radius, and T.B. Marder, “Palladium-Catalyzed Homocoupling of Highly                  Fluorinated Arylboronates: Studies of the Influence of Strongly vs. Weakly Coordinating Solvents on the Reductive Elimination                Process,” J. Am. Chem. Soc., 142: 6036-6050 (2020). DOI: 10.1021/jacs.9b11871. Read more...

    355. W. Ming, X. Liu, A. Friedrich, J. Krebs, Y.P. Budiman, M. Huang, and T.B. Marder, “Concise synthesis of α-amino cyclic boronates              via multicomponent coupling of salicylaldehydes, amines, and B2(OH)4,” Green Chem. 22: 2184-2190 (2020). DOI:                                       10.1039/D0GC00346H. Read more...

    354. X. Liu, W. Ming, X. Luo, A. Friedrich, J. Maier, U. Radius, W.L. Santos, and T.B. Marder, “Regio- and Stereoselective Synthesis of                 1,1-Diborylalkenes via Brønsted Base-Catalyzed Mixed Diboration of Alkynyl Esters and Amides with BpinBdan,” Eur. J. Org.                     Chem. 13: 1941-1946 (2020). DOI: 10.1002/ejoc.202000128. Read more...

    353. Q. Lu, G.K. Kole, A. Friedrich, K. Müller-Buschbaum, Z.-Q. Liu, X.-Q. Yu, and T.B. Marder, “Comparison Study of the Site-Effect on                Regioisomeric Pyridyl Pyrene Conjugates: Synthesis, Structures, and Photophysical Properties,” J. Org. Chem., 85: 4256-4266                  (2020). DOI: 10.1021/acs.joc.9bo3421. Read more...

    352. H. Amini, Ž. Ban, M. Ferger, S. Lorenzen, F. Rauch, A. Friedrich, I. Crnolatac, A. Kenđel, S. Miljanić, I. Piantanida, and T.B. Marder,                "Tetracationic bis-triarylborane 1,3-butadiyne as a combined fluorimetric and Raman probe for simultaneous and selective                      sensing of various DNA, RNA and proteins,” Chem. Eur. J., 26: 6017 –6028 (2020). DOI: 10.1002/chem.201905328.                                    Read more...

    351. F. Rauch, S. Fuchs, A. Friedrich, D. Sieh, I. Krummenacher, H. Braunschweig, M. Finze, and T.B. Marder, “Highly stable, readily                    reducible, fluorescent, trifluoromethylated 9-borafluorenes,” Chem. Eur. J., 26: 12794-12808 (2020).                                                                DOI: 10.1002/chem.201905559. Read more...

             (Designated as a Very Important Paper).

    350. W. Ming, X. Liu, A. Friedrich, J. Krebs, and T.B. Marder, “The Borono-Strecker Reaction: Synthesis of α-Aminoboronates via a                     Multicomponent Reaction of Carbonyl Compounds, Amines and B2pin2, ” Org. Lett., 22: 365-370 (2020). DOI:                                               10.1021/acs.orglett.9b03773. Illustrated on the cover: http://pubs.acs.org/toc/orlef7/22/2. Read more...

    349. Ž. Ban, S. Griesbeck, S. Tomić, J. Nitsch, T.B. Marder, and I. Piantanida, “A quadrupolar bis-triarylborane chromophore as a                        fluorimetric and  chirooptic probe for simultaneous and selective sensing of DNA, RNA and proteins,” Chem. Eur. J.,                                   26: 2195-2203 (2020). DOI: 10.1002/chem.201903936.

             (Designated as a Hot Paper).

             Featured in ChemistryViews:             

    https://www.chemistryviews.org/details/ezine/11223438/Simultaneous_and_Selective_Detection_of_DNARNA_and_Proteins.html

    348. H. Belaidi, F. Rauch, Z. Zhang, C. Latouche, A. Boucekkine, T.B. Marder, and J.-F. Halet, “Insights into the Optical Properties of                  Triarylboranes with Strongly Electron-accepting Bis(fluoromesityl)boryl Groups: When Theory Meets Experiment,”                                      ChemPhotoChem 4: 173-180 (2020). DOI: 10.1002/cptc.201900256. Read more...

    347. J. Merz, M. Dietz, Y. Vonhausen, F. Wöber, A. Friedrich, D. Sieh, I. Krummenacher, H. Braunschweig, M. Moos, M. Holzapfel,                      C. Lambert, and T.B. Marder, “Synthesis, Photophysical and Electronic Properties of New Red to NIR Emitting Donor-Acceptor                 Pyrene Derivatives,” Chem. Eur. J. 26: 438-453 (2020). DOI: 10.1002/chem.201904219. For cover image, see: DOI:                                      10.1002/chem.201905033. (Designated as a Hot Paper). Read more...

    346. X. Liu, W. Ming, A. Friedrich, F. Kerner, and T.B. Marder, "Copper-Catalyzed Triboration of Terminal Alkynes Using B2pin2: Efficient              Synthesis of 1,1,2- Triborylalkenes," Angew. Chem. Int. Ed. 59: 304-309 (2020). DOI: 10.1002/anie.201908466; Angew.                               Chem. 132: 311-316 (2020). DOI: 10.1002/ange.201908466. Read more...


    345. X. Liu, W. Ming, Y. Zhang, A. Friedrich, and T.B. Marder, "Copper-Catalyzed Triboration: Straightforward, Atom-Economical                         Synthesis of 1,1,1-Triborylalkanes from Terminal Alkynes and HBpin," Angew. Chem. Int. Ed. 58: 18923-18927 (2019). DOI:                       10.1002/anie.201909376; Angew. Chem. 131: 19099-19103 (2019). DOI: 10.1002/ange.201909376. Read more...

    344. S. Mueller, J. Lüttig, P. Malý, L. Ji, A. Dreuw, M. Moos, C. Lambert, U. Bunz, T.B. Marder, J. Han, and T. Brixner, “Rapid Multiple-                    quantum Three-dimensional Fluorescence Spectroscopy Disentangles Quantum Pathways,” Nature Comm. 10: 4735 (2019)                   DOI: 10.1038/s41467-019-12602-x. Read more...

    343. C. Lenczyk, D.K. Roy, K. Oberdorf, J. Nitsch, R.D. Dewhurst, K. Radacki, J.-F. Halet, T.B. Marder, F.M. Bickelhaupt, and H.                               Braunschweig, “Toward Transition-Metal-Templated Construction of Arylated B4 Chains by Dihydroborane Dehydrocoupling,”                  Chem. Eur. J. 25: 16544-16549 (2019). DOI: 10.1002/chem.201904772. Read more...

    342. J. He, F. Rauch, A. Friedrich, S. Sieh, T. Ribbeck, I. Krummenachaer, H. Braunschweig, M. Finze, and T.B. Marder, “N-Heterocyclic               Olefins as Electron Donors in Combination with Triarylborane Acceptors: Synthesis, Optical and Electronic Properties of D-p-A                Compounds,” Chem. Eur. J. 25: 13777-13784 (2019). DOI: 10.1002/chem.201903118. Read more...

    341. C. Lenczyk, D.K. Roy, J. Nitsch, K. Radacki, F. Rauch, R.D. Dewhurst, F.M. Bickelhaupt, T.B. Marder, and H. Braunschweig, “Steric                Effects Dicate the Formation of Terminal Arylborylene Complexes of Ruthenium from Dihydroboranes,” Chem. Eur. J., 25:                       13566-13571 (2019). DOI: 10.1002/chem.201902890. (Designated as a Hot Paper). Read more...

    340. Y.P. Budiman, A. Friedrich, U. Radius, and T.B. Marder, “Copper-Catalysed Suzuki-Miyaura Cross-
             Coupling of Highly Fluorinated Aryl Boronate Esters with Aryl Iodides and Bromides; Fluoroarenearene
             π-Stacking Interactions in the Products,” invited paper for special issue on “New Concepts in
             Homogeneous Catalysis,” ChemCatChem, 11: 5387-5396 (2019). DOI: 10.1002/cctc.201901220.

    339. S. Griesbeck, E. Michail, F. Rauch, H. Ogasawara, C. Wang, Y. Sato, R. Edkins, Z. Zhang, M. Taki, C. Lambert, 
             S. Yamaguchi, and T.B. Marder, "The Effect of Branching on One- and Two-Photon Absorption, Cell Viability
             and Localization of Cationic Triarylborane Chromophores with Dipolar vs. Octupolar Charge Distributions
             for Cellular Imaging," Chem. Eur. J., 25: 13164-13175 (2019). DOI: 10.1002/chem.201902461. Read more...

    338. T. Sick, J.M. Rotter, S. Reuter, S. Kandambeth, N.N. Bach, M. Döblinger, J. Merz, T. Clark, T.B.
             Marder, T. Bein, and D.D. Medina, “Switching On and Off Interlayer Correlations and Porosity in 2D
             Covalent Organic Frameworks,” J. Am. Chem. Soc.:  12570-12581 (2019). DOI: 10.1021/jacs.9b02800. Read more...

    337. N.I. Zahid, L. Ji, M.F. Khyasudeen, A. Friedrich, R. Hashim, T.B. Marder, and O.K. Abou-Zaid,
             “Evidence of Increased Hydrophobicity and Dynamics inside the Tail Region of Glycolipid Self-
             Assemblies Using 2-n-Alkyl-Pyrene Derivatives to Probe Different Locations,” Langmuir:  9584-9592 (2019).
             DOI: 10.1021/acs.langmuir.9b01767.

    336. J. Merz, A. Steffen, J. Nitsch, J. Fink, C.B. Schürger, A. Friedrich, I. Krummenacher, H.
             Braunschweig, M. Moos, D. Mims, C. Lambert, and T.B. Marder, “Synthesis, Photophysical and
             Electronic Properties of Tetra- Donor- or Acceptor-Substituted ortho-Perylenes Displaying Four
             Reversible Oxidations or Reductions,” Chem. Sci.:  7516-7534 (2019). DOI: 10.1039/c9sc02420d. Read more...

    335. L. Kuehn, M. Stang, S. Würtemberger-Pietsch, A. Friedrich, H. Schneider, U. Radius, and T.B.
            Marder, “FBpin and its Adducts and their Role in Catalytic Borylations,” Faraday Discuss., (2019).
            DOI: 10.1039/C9FD00053D. For the Faraday Discussion on Mechanistic Processes in Organometallic
            Chemistry, York, UK, September 2019.

    334. X. Jia, J. Nitsch, L. Ji, Z. Wu, A. Friedrich, F. Kerner, M. Moos, C. Lambert, and T.B. Marder
            “Triarylborane-Based Helical Donor-Acceptor Compounds: Synthesis, Photophysical and Electronic
            Properties,” Chem. Eur. J.:  10845-10857 (2019). DOI: 10.1002/chem.201902258. (Designated as a Hot Paper). Read more...

    333. L. Kuehn, D.G. Jammal, K. Lubitz, T.B. Marder, and U. Radius, “Stoichiometric and Catalytic Aryl-Cl
            Activation and Borylation using NHC-stabilized Nickel(0) Complexes,” invited paper for special
            OMCOS 20 issue, Chem. Eur. J.:  9514-9521 (2019). DOI: 10.1002/chem.201900937. (Designated as a Hot
            Paper).

    332. L. Kuehn, M. Huang, U. Radius and T.B. Marder, “Copper-Catalysed Borylation of Aryl Chlorides,”
             invited paper for special issue on Organoboron Chemistry, Org. Biomol. Chem. 17: 6601-6606
            (2019). DOI: 10.1039/C9OB01244C. Part of Themed Collections: Catalysis & biocatalysis in
            OBC; Organic and Biomolecular Chemistry HOT article collections; and Trends in
            Organoboron Chemistry
    .

    331. L. Ji, S. Hahn, P. Biegger, H. Reiss, J. Han, A. Friedrich, I. Krummenacher, H. Braunschweig, M.
            Moos, J. Freudenberg, C. Lambert, A. Dreuw, T.B. Marder, and U.H.F. Bunz, “Mono- and
            Dianion of a Bis(benzobuta)tetraazapentacene Derivative,” Chem. Eur. J.: 9840-9845  (2019). DOI:
            10.1002/chem.201901982. (Designated as a Hot Paper).

    330. S. Griesbeck, E. Michail, C. Wang, H. Ogasawara, S. Lorenzen, L. Gerstner, T. Zhang, J. Nitsch, Y.
             Sato, R. Bertermann, M. Taki, C. Lambert, S. Yamaguchi, and T.B. Marder, “Tuning the pi-Bridge of
             Quadrupolar Triarylborane Chromophores for One- and Two-Photon Ecited Fluorescence Imaging of
             Lysosomes in Live Cells,” Chem. Sci. 10: 5405-5422 (2019). DOI: 10.1039/c9sc00793h. Read more...

    329. T.E. Stennett, P. Bissinger, S. Griesbeck, S. Ullrich, I. Krummenacher, M. Auth, A. Sperlich, M.
            Stolte, K. Radacki, C.-J. Yao, F. Würthner, A. Steffen, T.B. Marder, and H. Braunschweig, “Near-
            Infrared Quadrupolar Chromophores Combining Three-Coordinate Boron-Based Superdonor and
            Superacceptor Units,” Angew. Chem. Int. Ed. 58: 6449-6454 (2019) DOI: 10.1002/anie.201900889.
            Angew. Chem. 131: 6516-6521 (2019) DOI: 10.1002/ange.201900889.

    328. S. Griesbeck, M. Ferger, C. Czernetzki, C. Wang, R. Bertermann, A. Friedrich, M. Haehnel, D. Sieh, M.
            Taki, S. Yamaguchi, and T.B. Marder, “Optimization of Aqueous Stability versus pi-Conjugation in
            Tetracationic Bis(triarylborane) Chromophores: Applications in Live-Cell Imaging,” Chem. Eur. J.
            25: 7679 – 7688 (2019). DOI: 10.1002/chem.201900723. (Designated as a Hot Paper). Read more...

    327. D.R. Chisholm, R. Lamb, T. Pallett, V. Affleck, C. Holden, J. Marrison, P. O’Toole, P.D. Ashton, K.
            Newling, A. Steffen, A.K. Nelson, C. Mahler, R. Valentine, T.S. Blacker, A.J. Bain, J. Girkin, T.B.
            Marder, A. Whiting, and C.A. Ambler, “Photoactivated Cell-Killing Involving a Low Molecular
            Weight, Donor-Acceptor Diphenylacetylene,” Chem. Sci. 10: 4673-4683 (2019). DOI:
           10.1039/C9SC00199A.

    326. M. Meier, L. Ji, J. Nitsch, I. Krummenacher, A. Deissenberger, D. Auerhammer, M. Schaefer, T.B.  
            Marder, and H. Braunschweig, “Preparation and Characterization of a pi-Conjugated Donor-Acceptor
           System Containing the Strongly Electron-Accepting Tetraphenylborole Unit,” Chem. Eur. J. 25: 4707-
           4712 (2019). DOI: 10.1002/chem.201805454.

    325. L. Kuehn, A.F. Eichhorn, T.B. Marder, and U. Radius, “Copper(I) Complexes of N-Alkyl.substituted
           N-Heterocyclic Carbenes,” invited paper for Richard J. Puddephatt 75th birthday issue, J. Organomet.
           Chem. 81: 25-33 (2019). DOI: 10.1016/j.jorganchem.2018.11.032.


    324. Y.-M. Tian, X.-N- Guo, M. Kuntze-Fechner, I. Krummenacher, H. Braunschweig, U. Radius, A.
            Steffen, and T.B. Marder, “Selective Photocatalytic C-F Borylation of Polyfluoroarenes by Rh/Ni Dual
            Catalysis Providing Valuable Fluorinated Arylboronate Esters” J. Am. Chem. Soc. 140: 17612-17623
            (2018). DOI: 10.1021/jacs.8b09790.

    323. J. Gala de Pablo, D.R. Chisholm, A. Steffen, A.K. Nelson, C. Mahler, T.B. Marder, S.A. Peyman, J.M.
           Girkin, C.A. Ambler, A. Whiting, and S.D. Evans, “Tandem Fluorescence and Raman (fluoRaman)
           Characterisation of a Novel Photosensitzer in Colorectal Cancer Cell Line SW480,” Analyst 143:
           6113-6120 (2018). DOI: 10.1039/c8an01461b.

    322. J.H. Muessig, D. Prieschl, A. Dießenberger, R.D. Dewhurst, M. Dietz, J.O.C. Jimenez-Halla, A.
            Trumpp, S.R. Wang, C. Brunecker, A. Haefner, A. Gärtner, T. Thiess, J. Böhnke, K. Radacki, R.
            Bertermann, T.B. Marder, and H. Braunschweig, “Reactivity of Tetrahalo- and Difluorodiboranes(4)
            Towards Lewis Basic Platinum(0): Bis(boryl), Borylborato and Doubly Boryl-bridged Platinum
            Complexes,” J. Am. Chem. Soc. 140: 13056-13063 (2018). DOI: 10.1021/jacs.8b08428. Read more...

    321. H. Reiss, L. Ji, J. Han, S. Koser, O. Tverskoy, J. Freudenberg, F, Hinkel, M. Moos, A. Friedrich, I.
             Krummenacher, C. Lambert, H. Braunschweig, A. Dreuw, T.B. Marder, U.H.F. Bunz, “Bromination
             Improves the Electron Mobility of Tetraazapentacene,” Angew. Chem. Int. Ed., 57: 9543-9547 (2018).
             DOI: 10.1002/anie.201805728. Angew. Chem. 130: 9688-9692 (2018). DOI:
             10.1002/ange.201805728.

    320. L. Ji, I. Krummenacher, A. Frieddrich, A. Lorbach, M. Haehnel, K. Edkins, H. Braunschweig, and T.
             B. Marder, “Synthesis, Photophysical, and Electrochemical Properties of Pyrenes Substituted with
             Donors or Acceptors at the 4- or 4,9-Positions,” J. Org. Chem. 83: 3599-3606 (2018). DOI:
             10.1021/acs.joc.7b03227.


    319. L. Mao, R. Bertermann, S.G. Rachor, K.J. Szabó, and T. B. Marder, “Palladium-Catalyzed Oxidative
           Borylation of Allylic CH Bonds in Alkenes,” Org. Lett. 19:  6590–6593 (2017).
           DOI: 10./acs.orglett.7b03296.

    318. L. Mao, R. Bertermann, K. Emmert, K.J. Szabó, and T. B. Marder, “Synthesis of Vinyl, Allyl-, and 2-Boryl
           Allyl-Boronates via a Highly Selective Copper-Catalyzed Borylation of Propargylic Alcohols,” Org. Lett. 19:
            6586–6589 (2017). DOI: 10./acs.orglett.7b03294.

    317. L. Ji, A. Friedrich, I. Krummenacher, A. Eichhorn, H. Braunschweig, M. Moos, S. Hahn, F. Geyer, O.
           Tverskoy, J. Han, C. Lambert, A. Dreuw, T.B. Marder, and U.H.F. Bunz, “Preparation, Properties and
           Structures of the Radical Anions, and Dianions of Azapentacenes,” J. Am. Chem. Soc. 139: 15968-15976
          (2017). DOI: 10.1021/jacs.7b09460.

    316. A.F. Eichhorn, L. Kuehn, T.B. Marder, and U. Radius, “Facile Insertion of a Cyclic(amino) Carbene into the
           B-B Bond of Diboron(4) Reagents,” Chem. Commun. 53: 11694-11696 (2017).
           DOI: 10.1039/c7cc06302d.

    315. Z. Wang, Y. Zhou, T.B. Marder, and Z. Lin, “DFT Studies on Reactions of Boroles with Carbon Monoxide,”
           Org. Biomol. Chem. 15: 7019-7027 (2017). DOI: 10.1039/C7OB01475A.

    314. X. Song, Z. Zhang, S. Zhang, J. Wei, K. Ye, Y. Liu, T.B. Marder, and Y. Wang, “Geometric Shape
           Regulation and Non-covalent Synthesis of One-Dimensional Organic Luminescent Nano/Micro-Materials,” J.
    Chem. Lett. 8: 3711-3717 (2017). DOI: 10.1021/acs.jpclett.7b01643.

    313. J. Merz, J. Fink, A. Friedrich, I. Krummenacher, H.H. Al Mamari, S. Lorenzen, M. Hähnel, A. Eichhorn, M.
           Moos, M. Holzapfel, H. Braunschweig, C. Lambert, A. Steffen, L. Ji, and T.B. Marder, “Pyrene MO Shuffle –
           Controlling Excited State and Redox Properties by Changing the Nature of the Frontier Orbitals,” Chem.
           Eur. J.
    23: 13164-13180 (2017). DOI: 10.1002/chem.201702594.

    312. Z. Wang, Y. Zhou, W.H. Lam, R.D. Dewhurst, H. Braunschweig, T.B. Marder, and Z. Lin,  “DFT Studies of
           Dimerization Reactions of Boroles,” Chem. Eur. J. 23: 11587-11597 (2017).
           DOI: 10.1002/chem.201701737.

    311. A.F. Eichhorn, S. Fuchs, M. Flock, T.B. Marder, and U. Radius, “Reversible Oxidative Addition at Carbon,”
           Angew. Chem. Int. Ed., 56: 10209-10213 (2017) . DOI: 10.1002/anie.201701679. Angew. Chem.,  129:
          10343-10347 (2017). DOI: 10.1002/ange.201701679.

    310. O. Diamond and T.B. Marder, “Methodology and Applications of the Hexahydro-Diels-Alder (HDDA)
            Reaction,” Invited Review for special issue on “Novel p-Electron Molecular Scaffolds,” Org. Chem.
    , 4, 891-910 (2017). DOI: 10.1039/C7QO00071E.

    309. M. Eck, S. Würtemberger-Pietsch, A. Eichhorn, J.H.J. Berthel, R. Bertermann, U. Paul, H. Schneider,
           A. Friedrich, C. Kleeberg, U. Radius, and T.B. Marder, “B–B Bond Activation and NHC Ring-expansion
           Reactions of Diboron(4) Compounds, and Accurate Molecular Structures of B2(NMe2)4, B2eg2, B2neop2
           and B2pin2,” Dalton Trans., 46: 3661-3680 (2017).
           DOI: 10.1039/C7DT00334J.

    308. C. Sieck, D. Sieh, M. Sapotta, M. Haehnel, K. Edkins, A. Lorbach, A. Steffen, and T.B. Marder,
            “Convenient Synthetic Access to Fluorescent Rhodacyclopentadienesvia Ligand Exchange Reactions,”
            Invited paper for John Gladysz 65th birthday issue, J. Organomet. Chem., 847: 184-192 (2017).
            DOI: 10.1016/j.jorganchem.2017.02.028.

    307. L. Mao, K. Szabó, and T.B. Marder, “Synthesis of Benzyl-, Allyl-, and Allenyl-boronates via
           Copper-catalyzed Borylation of Alcohols,” Org. Lett., 19: 1204-1207 (2017).
           DOI: 10.1021/acs.orglett.7b00256.

    306.  M. Lübtow, I. Helmers, V. Stepanenko, R. Q. Albuquerque, T.B. Marder, and G. Fernandez,
            “Self-Assembly of 9,10-Bis(phenylethynyl)anthracene (BPEA) Derivatives: Influence of p-p and
            Hyrdogen Bonding Interactions on Aggregate Morphology and Self-Assembly Mechanism,”
            Chem. Eur. J., 23: 6198-6205 (2017). DOI: 10.1002/chem.201605989.

    305. F.K. Scharnagl, S.K. Bose, and T.B. Marder, “Acylboranes: Synthetic Strategies and Applications,”
           Invited Review, Org. Biomol. Chem., 15: 1738-1752 (2017). DOI: 10.1039/C6OB02425D.

    304. L. Ji, S. Griesbeck, and T.B. Marder, “Recent Developments in and Perspectives on
           Three-CoordinateBoron Materials: A Bright Future,” Invited Review, Chem. Sci., 8: 846-863 (2017).
           DOI: 10.1039/C6SC04245G.

    303. S.K. Bose, S. Brand, H.O. Omoregie, M. Haehnel, J. Maier, G. Bringmann, and T.B. Marder,
           “Highly Efficient Synthesis of Alkylboronate Esters via Cu(II)-Catalyzed Borylation of Unactivated
            Alkyl Bromides and Chlorides in Air,” ACS Catal., 6: 8332-8335 (2016). DOI: 10.1021/acscatal.6b02918.

    302. S. Griesbeck, Z. Zhang, M. Gutmann, T. Lühmann, R.M. Edkins, G. Clermont, A.N.
            Lazar, M. Haehnel, K. Edkins, A. Eichhorn, M. Blanchard-Desce, L. Meinel, and
            T.B. Marder, "Water-Soluble Triarylborane Chromophores for One- and Two-
            Photon Excited Fluorescence Imaging of Mitochondria in Cells," Chem. Eur. J.,
            22: 14701-14706 (2016). DOI: 10.1002/chem.201602639.

    301. S. Würtemberger-Pietsch, H. Schneider, T.B. Marder, and U. Radius, "Adduct
            Formation, B-H Activation and Ring Expansion at Room Temperature from
            Reactions of HBcat with NHCs," Chem. Eur. J., 22: 13032-13036 (2016).
            DOI: 10.1002/chem.201603328.

    300. L. Ji, M. Haehnel, I. Krummenacher, P. Biegger, F.L. Geyer, O. Tverskoy, M.
            Schaffroth, J. Han, A. Dreuw, T.B. Marder, and U.H.F. Bunz, "The Radical Anion
            and Dianion of Tetraazapentacene," Angew. Chem. Int. Ed., 55: 10498-10501
            (2016). DOI: 10.1002/anie.201603177. Angew. Chem., 128: 10654-10657 (2016).
            DOI: 10.1002/ange.201603177.

    299. E.C. Neeve, S.J. Geier, I.A.I. Mkhalid, S.A. Westcott, and T.B. Marder, "Diboron(4)
            Compounds: From Structural Curiosity to Synthetic Workhorse," Chem. Rev., 116:
            9091-9161 (2016). DOI: 10.1021/acs.chemrev.6b00193.

    298. Z. Zhang, Z. Wang, M. Haehnel, A. Eichhorn, R.M. Edkins, A. Steffen, A.
            Krueger, Y. Lin, and T.B. Marder, "Synthesis and Fluxional Behavior of Novel
            Chloroborole Dimers," Chem. Commun., 52: 9707-9710 (2016).
            DOI: 10.1039/C6CC04831E.

    297. J. Zhou, J.H.J. Berthel, M.W. Kuntze-Fechner, A. Friedrich, T.B. Marder, and U.
            Radius, "NHC Nickel-Catalyzed Suzuki-Miyaura Cross-Coupling Reactions of
            Arylboronate Esters with Perfluorobenzenes," J. Org. Chem., 80: 5789-5794
            (2016). DOI: 10.1021/acs.joc.6b01041.

    296. C. Sieck, M.G. Tay, M.-H. Thibault, R.M. Edkins, K. Costuas, J.-F. Halet, A.S.
            Batsanov, M. Haehnel, K. Edkins, A. Lorbach, A. Steffen, and T.B. Marder, "Reductive
            Coupling of Diynes at Rhodium Gives Fluorescent Rhodacyclopentadienes or
            Phosphorescent Rhodium 2,2'-Biphenyl Complexes," Chem. Eur. J., 22: 10523-10532
            (2016). DOI: 10.1002/chem.201601912.

    295. U.S.D. Paul, C. Sieck, M. Haehnel, K. Hammond, T.B. Marder, and U. Radius,
            "Useful for Comparison: Cyclic (Alkyl)(Amino)Carbene Complexes of Rhodium and
            Nickel and their Steric and Electronic Parameters," Chem. Eur. J., 22: 11005-11014
            (2016). DOI: 10.1002/chem.201601406.

    294. J. Zhou, M.W. Kuntze-Fechner, R. Bertermann, U.S.D. Paul, J.H.J. Berthel,
            A. Friedrich, Z. Du, T.B. Marder, and U. Radius, "Preparing (Multi)Fluoroarenes
            as Building Blocks for Synthesis: Nickel-Catalyzed Borylation of Polyfluoroarenes
            via C-F Bond Activation," J. Am. Chem. Soc., 138: 5250-5253 (2016).
            DOI: 10.1021/jacs.6b02337.

    293. A.S. Batsanov, J.A. Cabeza, M.G. Crestani, M.R. Fructos, P. García-Álvarez,
            M. Gille, Z. Lin, and T.B. Marder, "Fully Borylated Methane and Ethane by
            Ruthenium Mediated Cleavage and Coupling of CO," Angew. Chem. Int. Ed.
            55: 4707-4710 (2016). DOI: 10.1002/anie.201601121. Angew. Chem. 128:
            4785-4788 (2016). DOI: 10.1002/ange.201601121.

    292. S. Würtemberger-Pietsch, U. Radius, and T.B. Marder, "25 years of
            N-Heterocyclic Carbenes: Activation of Both Main-Group Element-Element
            Bonds and NHCs Themselves," Invited Dalton Perspective, Dalton Trans. 45:
            5880-5895 (2016). DOI: 10.1039/C5DT04106F.




    291. D. Chaiyaveij, A.S. Batsanov, M.S. Fox, T.B. Marder, and A. Whiting, "An
            Experimental and Computational Approach to Understanding the Reactions of Acyl
            Nitroso Compounds in [4+2] Cycloadditions," J. Org. Chem., 80: 9518-9534 (2015).
            DOI: 10.1021/acs.joc.5b01470. Lesen Sie mehr...

    290. S.K. Bose and T.B. Marder, "Metal-fee Catalytic Borylation of Carbon-Hydrogen 
            Bonds - A Leap Forward in C-H Functionalization," invited Perspective, Science,
            349: 473-474 (2015). DOI: 10.1126/science.aac9244. Lesen Sie mehr...

    289. Z. Zhang, R.M. Edkins, M. Haehnel, M. Wehner, A. Eichhorn, L. Mailänder, M. Meier,
            J. Brand, F. Brede, K. Müller-Buschbaum, H. Braunschweig, and T.B. Marder,
            "Taming the Beast: Fluoromesityl Groups Induce a Dramatic Stability Enhancement 
            in Boroles," Chem. Sci., 6: 5922-5927 (2015). DOI: 10.1039/C5SC02205C.
            Lesen Sie mehr...

    288. S.K. Bose, A. Deißenberger, A. Eichhorn, P.G. Steel, Z. Lin, and T.B. Marder, "Zinc-
            Catalyzed Dual C-X and C-H Borylation of Aryl Halides," Angew. Chem. Int. Ed., 54:
            11843-11847 (2015). DOI: 10.1002/anie.201505603. Angew. Chem. 127: 12009-
            12014 (2015). DOI: 10.1002/ange.201505603. Lesen Sie mehr...

    287. N. Arnold, H. Braunschweig, P.B. Brenner, M. Ali Celik, R.D. Dewhurst, M. Haehnel,
            T. Kramer, I. Krummenacher, and T.B. Marder, "Correlations and Contrasts in Homo-
            Heteroleptic Cyclic (Alkyl)(amino)carbene (CAAC)-Containing Pt0 Complexes," Chem.
            Eur. J., 21: 12357-12362 (2015). DOI: 10.1002/chem.201502048.
            Lesen Sie mehr...

    286. L. Ji, R.M. Edkins, A. Lorbach, I. Krummenacher, C. Brückner, A. Eichhorn, H.
            Braunschweig, B. Engels, P.J. Low, and T.B. Marder, "Electron Delocalization in
            Reduced Forms of 2-(BMes2)pyrene and 2,7-Bis(BMes2)pyrene," J. Am. Chem. Soc.,
            137: 6750-6753 (2015). DOI: 10.1021/jacs.5b03805. Lesen Sie mehr...

    285. L. Ji, A. Lorbach, R.M. Edkins, and T.B. Marder, "Synthesis and Photophysics of a
            2,7-Disubstituted Donor-Acceptor Pyrene Derivative: An Example of the Application
            of Sequential Ir-Catalyzed C-H Borylation and Substitution Chemistry," J. Org. Chem.,
            80: 5658-5665 (2015. DOI: 10.1021/acs.joc.5b00618. Lesen Sie mehr...

    284. S.A. Sadler, A. C. Hones, B. Roberts, D. Blakemore, T.B. Marder, and P.G. Steel,
            "Multidirectional Synthesis of Substituted Indazoles via Iridium-Catalyzed C-H
            Borylation," J. Org. Chem., 80: 5308-5314 (2015). DOI: 10.1021/acs.joc.5b00452.
            Lesen Sie mehr...

    283. S. Pietsch, U. Paul, I.A. Cade, M.J. Ingleson, U. Radius, and T.B. Marder, "Room
            Temperature Ring Expansion of N-Heterocyclic Carbenes and B-B Bond Cleavage of
            Diboron(4) Compounds," Chem. Eur. J., 21: 9018-9021 (2015).
            DOI: 10.1002/chem.201501498. Lesen Sie mehr...

    282. R.D. Dewhurst, E.C. Neeve, H. Braunschweig, and T.B. Marder, "sp²-sp³ Diboranes:
            Astounding Structural Variability and Mild Sources of Nucleophilic Boron for Organic
            Synthesis," Chem. Commun., 51: 9594-9607 (2015). (Featured Article).
            DOI: 10.1039/c5cc02316e. Lesen Sie mehr...

    281. M.S. Cheung, F.K. Sheong, T.B. Marder, and Z. Lin, "Computational Insight into
            Nickel-Catalyzed Carbon-Carbon versus Carbon-Boron Coupling Reactions of
            Primary, Secondary and Tertiary Alkyl Bromides," Chem. Eur. J., 21: 7480-7488
            (2015). DOI: 10.1002/chem.201500110. (Designated as a Hot Paper).
            Lesen Sie mehr...

    280. S. Pietsch, E.C. Neeve, D.C. Apperley, R. Bertermann, F. Mo, Di Qiu, M.S. Cheung, L.
            Dang, J. Wang, U. Radius, Z. Lin, C. Kleeberg, and T.B. Marder, "Synthesis, Structure
            and Reactivity of Anionic sp2-sp3 Diboron Compounds: Readily Accessible Boryl
            Nucleophiles," Chem. Eur. J., : 7082-7098 (2015). DOI: 10.1002/chem.201500235.
            (Designated as a Hot Paper). Lesen Sie mehr...

    279. L. Ji, K. Fucke, S.K. Bose, and T.B. Marder, “Iridium-Catalyzed Borylation of Pyrene:
            Irreversibility and the Influence of Ligand on Selectivity,” J. Org. Chem., 80: 661-665
            (2015). Lesen Sie mehr...

    278. Z. Zhang, R.M. Edkins, J. Nitsch, K. Fucke, A. Eichhorn, A. Steffen, Y. Wang, and
            T.B. Marder, “D-π-A Triarylboron Compounds with Tunable Push-Pull Character
            Achieved by Modification of Both the Donor and Acceptor Moieties,” Chem. Eur. J., 
            21: 177-190 (2015). DOI: 10.1002/chem.201405621. (Designated as a VIP – 
            Very Important Paper). Lesen Sie mehr...

    277. Z. Zhang, R.M. Edkins, J. Nitsch, K. Fucke, A. Steffen, L.E. Longobardi,
            D.W. Stephan, C. Lambert and T.B. Marder, “ Optical and Electronic Properties
            of Air-stable Organoboron Compounds with Strongly Electron-accepting
            Bis(fluoromesityl)boryl Groups,” Chem. Sci., 6: 308-321 (2015).
            DOI: 10.1039/c4sc02410a  Lesen Sie mehr... 

    276. Z.-Q. Zhang, C.-T. Yang, L.-J. Liang B. Xao, X. Lu, J.-H. Liu, Y.-Y. Sun, T.B. Marder,
            and Y. Fu, “Copper-Catalyzed/Promoted Cross-coupling of gem-Diborylalkanes
            with Nonactivated Primary Alkyl Halides: An Alternative Route to Alkylboronic
            Esters", Org. Lett., 16: 6342-6345 (2014). DOI: 10.1021/ol503111h.
           Lesen Sie mehr...

    275. S.A. Sadler, H. Tajuddin, I.A.I. Mkhalid, A.S. Batsanov, D. Albesa-Jove,
            M.S. Cheung, A.C. Maxwell, L. Shukla, B. Roberts, D.C. Blakemore, Z. Lin,
            T.B. Marder, and P.G. Steel, “Iridium-Catalyzed C-H Borylation of Pyridines,”
            Org. Biomol. Chem., 12: 7318-7327 (2014). DOI: 10.1039/C4OB01565G
            Lesen Sie mehr...

    274. S.K. Bose and T.B. Marder, “Efficient Synthesis of Aryl Boronates via Zinc-
            Catalyzed Cross-Coupling of Alkoxy Diboron Reagents with Aryl Halides at
            Room Temperature,” Org. Lett., 16: 4562-4565 (2014). DOI: 10.1021/ol502120q
            Lesen Sie mehr...

    273. L. Ji, R.M. Edkins, L.J. Sewell, A. Beeby, A.S. Batsanov, K. Fucke, M. Drafz,
            J.A.K. Howard O. Moutounet, F. Ibersiene, A. Boucekkine, E. Furet, Z. Liu,
            J.-F. Halet, C. Katan, and T.B.Marder, “Experimental and Theoretical Studies
            of Quadrupolar Oligothiophene-cored Chromophores Containing Dimesitylboryl
            Moieties as π-Accepting End-groups: Syntheses,Structures, Fluorescence,
            One- and Two-photon Absorption,” Chem. Eur. J., 20: 13618 13635 (2014).
            DOI: 10.1002/chem.201402273. Lesen Sie mehr...

    272. A. Steffen, K. Costuas, A. Boucekkine, M.-H. Thibault, A. Beeby, A.S. Batsanov,
            A. Charaf Eddin, D. Jacquemin, J.-F. Halet, and T.B. Marder, "Fluorescence in
            Rhoda- and Iridacyclopentadienes Neglecting the Spin-Orbit Coupling of the
            Heavy Atom: The Ligand Dominates" Inorg. Chem., 53: 7055-7069 (2014).
            DOI: 10.1021/ic501115k  Lesen Sie mehr...

    271. X. Yin, J. Chen, R.A. Lalancette, T.B. Marder, and F. Jäkle, “Highly Electron-
            Deficient, Air Stable Conjugated Thienylboranes,” Angew. Chem. Int.
            Ed., 53: 9761-9765 (2014). DOI: 10.1002/anie.201403700.
            Lesen Sie mehr...

    270. R. Dewhurst and T.B. Marder, “Cascades of Catalytic Selectivity,”
            invited News and Views paper,  Nature Chemistry, 6: 279-280 (2014).
            Lesen Sie mehr...

    269. A. Steffen, R.M. Ward, M.G. Tay, R.M. Edkins, F. Seeler, M. van Leeuwen,
            L.-O. Pålsson, A. Beeby, A.S. Batsanov, J.A.K. Howard, and T.B. Marder,
            “Regiospecfic formation and Unusual Optical Properties of 2,5-Bis(arylethynyl
            rhodacyclopentadienes: A New Class of Luminescent Organometallics,”
            Chem. Eur. J., 20: 3652-3666 (2014). DOI:10.1002/chem.201304068. 
            Lesen Sie mehr...

    268. R.E. Lopez-Real, J.J.R. Budge, T.B. Marder, A. Whiting, P.N. Hunt, and 
            S.A. Przyborski, “Application of Synthetic Photostable Retinoids Induces 
            Novel Limb and Facial Phenotypes During Chick Embryogenesis In Vivo,” 
            J. Anat., 224: 392-411 (2014). DOI: 10.1111/joa.12147. Lesen Sie mehr... 
            Corrigendum: J. Anat., 224: 529 (2014).  DOI: 10.1111/joa.12161. 

    267. S. Konishi, S. Kawamorita, T. Iwai, P.G. Steel, T.B. Marder, and M. Sawamura, 
            “Site-Selective C-H Borylation of Quinolines at the C8 Position Catalyzed by a Silica
            Supported Phosphane-Iridium System,” Chem. Asian J., 9: 434-438 (2014). 
            DOI: 10.1002/asia.201301423 Lesen Sie mehr...

    266. S.K. Bose, K. Fucke, L. Liu, P.G. Steel, and T.B. Marder, “Zinc-Catalyzed Borylation
            of Primary, Secondary and Tertiary Alkyl Halides with Alkoxy Diboron Reagents 
            at Room Temperature,” Angew. Chem. Int. Ed., 53: 1799-1803 (2014). 
            DOI: 10.1002/anie.201308855 (Designated as a Hot Paper).
            Lesen Sie mehr...

    265. J.A. Foster, R.M. Edkins, G.J. Cameron, N. Coglin, K. Fucke, S. Ridgeway, 
            A.G. Crawford, T.B. Marder, A. Beeby, S.L. Cobb, and J.W. Steed, 
           “Blending Gellators to Tune Gel Structure and Probe Anion-Induced Disassembly,” 
            Chem. Eur. J., 20: 279-291 (2014). DOI: 10.1002/chem.201303153
            Lesen Sie mehr...




    264. P.R. Matthes, J. Nitsch, A. Kuzmanoski, C. Feldmann, A. Steffen, T.B. Marder, 
            and K. Müller-Buschbaum, “ The Series of Rare Earth Complexes 
            [Ln2Cl6(m-4,4’-bipy)(py)6], Ln=Y, Pr, Nd, Sm-Yb: A Molecular Model System for
            Luminescence Properties in MOFs Based on LnCl3 and 4,4’-Bipyridine,”
            Chem. Eur. J., 19: 17369-17378 (2013). DOI: 10.1002/chem.201302504
            Lesen Sie mehr...

    263. G. Clemens, K.R. Flower, P. Gardener, A.P. Henderson, J.P. Knowles, T.B. Marder, 
            A. Whiting, and S.A. Przyborski, "Design and Biological Evaluation of Synthetic
            Retinoids: Probing Length vs. Stability vs. Activity," Mol. BioSyst., 9: 3124-3134
            (2013). DOI: 10.1039/c3mb70273a
            Lesen Sie mehr...

    262. H. Braunschweig, F. Guethlein, L. Mailänder, and T.B. Marder, "Synhesis of
            Catechol-, Pinacol-, and Neopentaneglyclborane via Heterogeeous Catalytic B-B
            Bond Hydrogenolysis of Diboranes(4)," Chem. Eur. J., early view (2013).
            DOI: 10.1002/chem.201302677
            Lesen Sie mehr...

    261. R.M. Edkins, K. Fucke, M.J.G. Peach, A.G. Crawford, T.B. Marder, and A. Beeby,
            "Syntheses, Structures and Comparison of the Photophysical Properties of
            Cyclometalated Iridium Complexes Containing the Isomeric 1- and 2-(2'-pyridyl)
            Pyrene Ligands," Inorg. Chem. 52: 9842-9860 (2013). DOI: 10.102/ic400819f
            Lesen Sie mehr...

    260. G.L. Zhou, D.M. Tams, T.B. Marder, R. Valentine, A. Whiting, and S. Przyborski,
            "Synthesis and Applications of 2,4-Sisubstituted Thiazole Derivatives as Small 
            Molecule Modulators of Cellular Development," Org. Biomol. Chem., 11:
            2323-2334 (2013). DOI: 10.1039/C3OB00005B (Designated as a Hot Article).
            Lesen Sie mehr...       

    259. M.-H. Thibault, M.G. Tay, A.S. Batsanov, J.A.K. Howard, and T.B. Marder,
            “Oxidative Addition of (Bromoethynyl)benzen to
            k²-Acetylacetonatobis(trimethylphosphine)rhodium(I),” invited paper for
            ICOMC/F.G.A. Stone Special Issue, J. Organomet. Chem. 730: 104-107 (2013).
            DOI: 10.1016/j.jorganchem.2012.11.19.
            Lesen Sie mehr...

    258. H. Tajuddin, P. Harrisson, B. Bitterlich, J.C. Collings, N. Sim, A.S. batsanov,
            M.S. Cheung, S. Kawamorita,A.C. Maxwell, L. Shukla, J. Morris, Z. Lin, T.B. Marder,
            and P.G. Steel, “Iridium-Catalyzed C-H Borylation of Quinolines and Substituted
            Benzenes: Insights Into Steric and Electronic Effects on Selectivity,”
            Chem. Sci., 3: 3505-3515 (2012). DOI: 10.1039/c2sc20776a.
            Lesen Sie mehr...

    257. A.S. Batsanov, J.A.K. Howard, N. Wu, Z. Yang, and T.B. Marder, “An Irreversible
            Phase Transition in 1-n-butylindeno[2,1,c]pyran-3,9-dione,” Acta Crystallogr.,
            C68: o413-o416 (2102). DOI: 10.1107/S010827011203805X.
            Lesen Sie mehr...

    256. N. Wu, A. Messinis, A.S. Batsanov, Z. Yang, A. Whiting, and T.B. Marder,
            “Palladium(II)-Catalysed Tandem Cyclisation of Electron-Deficient Aromatic Enynes,”
            Chem. Commun., 48: 9986-9988 (2012). DOI: 10.1039/C2CC35114E.
            Lesen Sie mehr...

    255. Z. Liu, Y. Wang, Y. Chen, J. Liu, Q. Fang, C. Kleeberg, and T.B. Marder, “Ir-Catalyzed
            Direct Borylation at the 4-Position of Pyrene,” J. Org. Chem., 77: 7124-7128 (2012).
            Lesen Sie mehr...

    254.  A.S. Batsanov, J.A.K. Howard, D. Albesa-Jové, J.C. Collings, Z. Liu, I.A.I. Mkhalid,
            M.-H. Thibault and T.B. Marder, “Structural Versatility of Pyrene-2-(4,4,5,5
            tetramethyl-[1,3,2]dioxaborolane) and Pyrene 2,7-bis(4,4,5,5
            tetramethyl-[1,3,2]dioxaborolane)” Cryst. Growth Des., 12: 2794-2802.
            DOI: 10.1021/cg201554t.
            Lesen Sie mehr...

    253.  B. Liu, M. Gao, L. Dang, H. Zhao, T. B. Marder, and Z. Lin, “DFT Studies on the
            Mechanisms of the Platinum-Catalyzed Diboration of Acyclic alpha,beta-Unsaturated
            Carbonyl Compounds,” Organometallics, 31: 3410-3425, (2012).
            Lesen Sie mehr...

    252.  A.G. Crawford, Z. Liu, I.A.I. Mkhalid, M.-H. Thibault, N. Schwarz, G. Alcaraz,
            A. Steffen, J.C. Collings, A.S. Batsanov, J.A.K. Howard, and T.B. Marder, “Synthesis
            of 2- and 2,7-Functionalized Pyrene Derivatives: An Application of Selective
            C–H Borylation,” Chem. Eur. J., 18: 5022-5035 (2012).
            Lesen Sie mehr...

    251.  L. Weber, D. Eickhoff, T.B. Marder, M.A. Fox, P.J. Low, A.D. Dwyer, D.J. Tozer,
            S. Schwedler, A. Brockhinke, H.G. Stammler, and B. Neumann, “Experimental and
            Theoretical Studies on Organic D-Pi-A Systems Containing 3-Coordinate Boron
            Moieties as Both Pi-Donor and Pi-Acceptor,” Chem. Eur. J., 18: 1369-1382 (2012).
            DOI: 10.1002/chem.201102059.
            Lesen Sie mehr...

    250.  C. Kleeberg, A.G. Crawford, A.S. Batsanov, P. Hodgkinson, D.C. Apperley,
            M.S. Cheung, Z.Y. Lin and T.B. Marder, “Spectroscopic and Structural
            Characterization of the CyNHC Adduct of B2pin2 in Solution and in the Solid State,”
            J. Org. Chem., 77: 785-789 (2012). DOI: 10.1021/jo202127
            Lesen Sie mehr...

    249.  C.-T. Yang, Z.-Q. Zhang, H. Tajuddin, C.-C. Wu, J. Liang, J.-H. Liu, Y.F.,
            M. Czyzewska, P.G. Steel, T.B. Marder, and L. Liu, “Alkylboronic Esters from
            Copper-Catalyzed Borylation of Primary and Secondary Alkyl Halides and
            Pseudo-Halides,” Angew. Chem. Int. Ed., 51: 528-532 (2012).
            DOI: 10.1002/anie.201106299.
            Lesen Sie mehr...
    248.  J. Zheng, S. Lin, B.-W. Jiang, T.B. Marder, and Z. Yang, “The Role of the Magnetic
            Nanoparticles (MNP) as Reducing Agent in an MNP-Supported Pd-Catalyst for the
            Reductive Homocoupling of Aryl Halides,” special issue for T.-H. Chan,
            Can. J. Chem., 90: 138-144 (2012). DOI: 10.1002/chin.201225085.
            Lesen Sie mehr...

    247.  C. Kleeberg, M.S. Cheung, Z. Lin, and T.B. Marder, “A Copper Mediated Reduction of
            CO2 with pinB–SiMe2Ph via CO2 Insertion into a Copper-Silicon Bond,”
            J. Am. Chem. Soc.,133: 19060-19063 (2011).
           Lesen Sie mehr...
    246.  A.G. Crawford, A.D. Dwyer, Z. Liu, A. Steffen, A. Beeby, L.-O. Pålsson, D.J. Tozer,
            and T.B. Marder, “Experimental and Theoretical Studies of the Photophysical
            Properties of 2- and 2,7-Functionalized Pyrene Derivatives,” J. Am. Chem. Soc.,
            133:13349-13362 (2011).
             Lesen Sie mehr...
    245.  J.B. Bauer, W.P. Lippert, S. Dörrich, D. Tebbe C. Burschka, V.B. Christie,
            B.A. Murray, T.B. Marder, S.A. Przyborski, and R Tacke, “Novel Silicon-Containing
            Analogues of the Retinoid Agonist Bexarotene: Syntheses and Biological Effects
            on Human Pluripotent Stem Cells,” Chem. Med. Chem., 6: 1509-1517 (2011).
            Lesen Sie mehr...

    244.  D. Chaiyaveij, L. Cleary, A.S. Batsanov, T.B. Marder, K.J. Shea, and A. Whiting,
            “Copper(II)-Oxazoline Catalyzed Room Temperature Aerobic Oxidation of
            Hydroxamic Acids and Hydrazides to Acyl-Nitroso and Azo Intermediates,
            and their Diels­–Alder Trapping,” Org. Lett., 13: 3442-3445 (2011).
            Lesen Sie mehr...

    243.  M.S Cheung, T.B. Marder, and Z. Lin, “Mechanisms of Reactions of Lithium Boryl
            with Organohalides,” Organometallics, 30: 3018-3028 (2011).
            Lesen Sie mehr...
    242.  M. Gao, S.B. Thorpe, C. Kleeberg, C. Slebodnick, T.B. Marder, and W. Santos,
            “Structure and Reactivity of a Preactivated sp2-sp3 Diboron Reagent: Catalytic
            Regioselective Boration of a,b-Unsaturated Conjugated Compounds,”
            J. Org. Chem., 76: 3997-4007 (2011).
            Lesen Sie mehr...
    241.  H. Tajuddin, L. Shukla, A.C. Maxwell, T.B. Marder, and P.G. Steel, “A “One-Pot”
            Tandem C-H Borylation/1,4-Conjugate Addition/Reduction Sequence,”
            Org. Lett., 12: 5700-5703 (2010).
            Lesen Sie mehr...
    240.  J.L. Palma, E. Atas, L. Hardison, T.B. Marder, J.C. Collings, A. Beeby, J.S. Melinger,
            J.L. Krause, V.D. Kleiman, and A.E. Roitberg, “Electronic Spectra of the Nanostar
            Dendrimer: Theory and Experiment,” J. Phys. Chem. C, 114: 20702-20712 (2010).
            Lesen Sie mehr...

    239.  V.B. Christie, D.J. Maltman, A. Whiting, T.B. Marder, and S.A. Przyborski,
            “Retinoid Supplementation Leads to Increased Neuronal Maturity During
            Differentiation of a Commercial Human Neural Progenitor Cell Line,”
            J. Neurosci. Methods, 193: 239-245 (2010).
           Lesen Sie mehr...

    238.  Y.-X. Gao, L. Chang, H. Shi, B. Liang, K. Wongkhan, D. Chaiyaveij, A.S. Batsanov,
            T.B. Marder, C.-C. Li, Z. Yang and Y. Huang, “A Thiourea-oxazoline Library with
            Axial Chirality: Ligand Synthesis and Studies of the Palladium-Catalyzed
            Enantioselective Bis(methoxycarbonylation) of Terminal Olefins,” Adv. Synth. Catal.,
            352: 1955-1966 (2010).
            Lesen Sie mehr...

     237.  A. Steffen, R.M. Ward, W.D. Jones, and T.B. Marder, “Dibenzometall-
             acyclopentadienes, Boroles and Selected Transition Metal and Main Group
             Heterocyclopentadienes: Synthesis, Catalytic and Optical Properties,”
             Coord. Chem. Rev., 254: 1950-1976 (2010).
             Lesen Sie mehr...

    236.  T.E. Hurst, T.K. Macklin, M. Becker, E. Hartmann, W. Kügel, J.-C. Parisienne-
            La Salle, A.S. Batsanov, T.B. Marder, and V. Snieckus, “Iridium-Catalyzed C-H
            Activation versus Directed ortho Metalation (DoM): Complementary Borylation
            of Aromatics and Heteroaromatics,” Chem. Eur. J., 16: 8155-8161 (2010).
            Lesen Sie mehr...

    235.  K.C. Lam, T.B. Marder, and Z. Lin, “Mechanism of the Palladium-Catalyzed Borylation
            of Aryl Halides with Pinacolborane,” Organometallics, 29: 1849-1857 (2010).
            Lesen Sie mehr...

    234.  L. Dang, Z. Lin, and T.B. Marder, “DFT Studies on the Carboxylation of Arylboronate
            Esters with CO2 Catalyzed by Copper(I) Complexes,” Organometallics, 29: 917-92
            Lesen Sie mehr...

    233.  A. Steffen, M.G. Tay, A.S. Batsanov, J.A.K. Howard, A. Beeby, K.Q. Vuong,
            X.-Z. Sun, M.W. George, and T.B. Marder, “2,5-Bis(p-Arylethynyl)-
            Rhodacyclopentadienes Show Intense Fluorescence: Denying the Presence
            of a Heavy Atom,” Angew. Chem. Int. Ed., 49: 2349-2353 (2010).
           Lesen Sie mehr...

    232.  Q. Li, K. Wongkhan, X. Luo, A.S. Batsanov, J.A.K. Howard, Y. Lan, Y. Wu, A. Lei,
            and T.B. Marder, “A Novel Self-Promoted Morita-Baylis-Hillman-Like Dimerisation,”
            invited paper, Chinese Science Bull., 55: 2794-2798 (2010).
            Lesen Sie mehr...

    231.  I.A.I. Mkhalid, J.H. Barnard, T.B. Marder, J.M. Murphy, and J.F. Hartwig,
            “C-H Activation for the Construction of C-B Bonds,” invited review, Chem. Rev.,
            110: 890-931 (2010).
             Lesen Sie mehr...

    230.  H.M. Colquhoun, Z. Zhu, D.J. Williams, M.G.B. Drew, C.J. Cardin, Y. Gan,
            A.G. Crawford, and T.B. Marder, “Induced-fit Binding of p-Electron Donor
            Substrates to Macrocyclic Aromatic Ether-imide-sulfones: A Versatile Approach to
            Molecular Assembly,” Chem. Eur. J., 16: 907-918 (2010).
            Lesen Sie mehr...



         Archiv 2009-2008    

         Archiv 2007-2006     

         Archiv 2005-2004

         Archiv 2003-2000

         Archiv 1999-1995

         Archiv 1994-1990

         Archiv 1989-1985

         Archiv 1984-1980

    Bücher, Papers, Reports

    Book Chapters

    1.         T.B. Marder, “Diborane(4) Compounds,” in Science of Synthesis, Houben-Weyl Methods of Molecular Transformations, Volume 6 - Boron Compounds, D. Kaufmann and D.S. Matteson, eds., Chapter 6.1.3, pp. 117-137, Georg Thieme Verlag, Stuttgart, 2004.

    Book Reviews

    2.         Descriptive Inorganic Chemistry, 2nd Edition, by G. Rayner-Canham, W.H. Freeman, 1999.
    In Educ. Chem. 37: 139 (2000).

     1.        Mechanisms of Inorganic and Organometallic Reactions, Vol. 6, M.V. Twigg, ed., Plenum Press, 1989.
    In American Scientist 79: 471-472 (1991).

    Other Invited Papers

     1.        T.B. Marder, "Molecular Materials for Nonlinear Optics," Canadian Chemical News, 44: No. 10 (Nov./Dec.), 22-23 (1992).

    Other Papers and Reports

     1.        A. Beeby, K.S. Findlay, P.J. Low, T.B. Marder, S.R. Rutter, P. Matousek, A.W. Parker, and M. Towrie, “Studies of the S1 State in a Prototypical Molecular Wire Using Picosecond Time-resolved Spectroscopies,” Central Laser Facility, CCLRC, Rutherford Appleton Laboratory, Annual Report, 2002-2003, 119-121.

    Books Edited

    2.         T.B. Marder and Z. Lin (Eds.), “Contemporary Metal Boron Chemistry I: Borylenes, Boryls, Borane Sigma-Complexes, and Borohydrides,” Structure and Bonding, Volume 130, Springer, Heidelberg, May 2008 (218 pages).

     1.         M.G. Davidson, A.K. Hughes, T.B. Marder, and K. Wade (Eds.), "Contemporary Boron Chemistry," Spec. Publ. No. 253, The Royal Society of Chemistry, Cambridge, 2000.

    Journal Issues Edited

    3.         T.B. Marder, P.W.Dyer, I.J.S. Fairlamb, S. Gibson, P. Scott, “Dalton Discussion 12: Catalytic C-H and C-X Bond Activation (DD12),” Dalton Trans., 39: 10335-10337 (2010), editorial introduction to Dalton Transactions themed issue 43, pages 10321-10540.

    2.         T.B. Marder (Guest Editor), Dalton Transactions, 2008: “Collection of articles dedicated to Professor Ken Wade, F.R.S. in celebration of his seventy-fifth birthday.”

    1.          T.B. Marder, Editorial for special issue of Journal of Organometallic Chemistry: “Frontiers in Boron Chemistry, Dedicated to Professor M. Frederick Hawthorne in Celebration of his 75th Birthday,” J. Organometal. Chem., 680: 1-2 (2003).

    Patent Applications

    Patents: 7 applications submitted, 1 granted thus far, 6 pending

    1. Stefan Przyborski, Andrew Whiting, Todd Marder, “Retinoid compounds and their use”,
        CA2662218 A1, PCT/GB2007/003237, Mar. 6, 2008, Pending

    2. Todd Marder , Stefan Przyborski, Andrew Whiting, “Retinoid compounds and their use”,
        WO2008025965 A3, PCT/GB2007/003237, Oct. 2, 2008, Pending

    3. Todd Marder , Stefan Przyborski, Andrew Whiting, “Retinoid compounds and their use”,
        EP2054504 A2, May 6, 2009, Pending

    4. Stefan Przyborski, Andrew Whiting, Todd Marder, “Retinoid compounds and their use”,
        EP2130908 A3, Jan. 6, 2010, Pending

    5. Stefan Przyborski, Andrew Whiting, Todd Marder, “Retinoid compounds and their use”,
        US20100093088 A1, PCT/GB2007/003237, Apr. 15, 2010, Pending

    6. Todd Marder , Stefan Przyborski, Andrew Whiting, “Retinoid compounds and their use”,
         WO2012076842 A1, PCT/GB2007/003237, Jun. 14, 2012, Pending

    7. Stefan Przyborski, Andrew Whiting, Todd Marder, “Synthetic retinoids for control of cell
        differentiation”, US8293803 B2, PCT/GB2007/003237, Oct. 23, 2012, Issued

    8. Andrew Whiting, Todd Marder, “Fluorescent synthetic retinoids,” CA2962150A1, EP3204357A2,
        WO2016055800A2, WO2016055800A3, US20170217893 A1, PCT/GB2015/052956, Oct 9, 2015,
        CN107250112 (A), publication date: 2017-10-13;
        AU2015329798 (A1), 2017-05-11;
        CA2962150 (A1), 2016-04-14;
        JP2017537140 (A), 2017-12-14;
        EP3204357 (A2), 2017-08-16;
        US2017217893 (A1), 2017-08-03;
        WO2016055800 (A2), 2016-04-14.