Marder Group

    The latest publications


    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.
    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    








    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 Scientist79: 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

    2.          University of Durham, A.P. Henderson, J.P. Knowles, A. Whiting, S. Przyborski, and T.B. Marder, “Synthetic Retinoids with Natural Retinoid Properties for Selective and Controllable Stem Cell Differentiation,” GB1020848.6.

     1.         University of Durham, S. Przyborski, A. Whiting, and T.B. Marder, (WO/2008/025965), “Retinoid Compounds and their Use,” PCT/GB2007/003237. (The invention relates to retinoid compounds of the formula (I): wherein V is a hydrophobic group; W is a non-polyenic linker; and X is a polar group comprising a hydrogen bond donor; or a salt thereof, and to the use of such compounds in the control of cell differentiation.)

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