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Pure Appl. Chem., 1999, Vol. 71, No. 8, pp. 1443-1452

http://dx.doi.org/10.1351/pac199971081443

The bite angle makes the catalyst

P. W. N. M. van Leeuwen, P. C. J. Kamer and J. N. H. Reek

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  • Sues Peter E., Lough Alan J., Morris Robert H.: A sulfur mimic of 1,1-bis(diphenylphosphino)methane: a new ligand opens up. Chem. Commun. 2014, 50, 4707. <http://dx.doi.org/10.1039/c3cc49456j>
  • Papp Tamara, Kollár László, Kégl Tamás: Estimation of Bite Angle Effect on the Electronic Structure of Cobalt-Phosphine Complexes: A QTAIM Study. Journal of Quantum Chemistry 2014, 2014, 1. <http://dx.doi.org/10.1155/2014/528072>
  • Christl Josefine T., Roesle Philipp, Stempfle Florian, Wucher Philipp, Göttker-Schnetmann Inigo, Müller Gerhard, Mecking Stefan: Catalyst Activity and Selectivity in the Isomerising Alkoxycarbonylation of Methyl Oleate. Chem. Eur. J. 2013, 19, 17131. <http://dx.doi.org/10.1002/chem.201301124>
  • Naik Susmita, Mague Joel T., Balakrishna Maravanji S.: N1,N1,N4,N4-Tetrakis(dibenzylphosphino)benzene-1,4-diamine: Synthesis, structural studies and transition metal chemistry. Inorganica Chimica Acta 2013, 407, 139. <http://dx.doi.org/10.1016/j.ica.2013.07.026>
  • Chacko Aneesh, Idem Ubong R., Bains Chatin H., Mihichuk Lynn M., East Allan L. L.: Bite Angle Effects of κ2P-dppm vs κ2P-dppe in Seven-Coordinate Complexes: A DFT Case Study. Organometallics 2013, 32, 5374. <http://dx.doi.org/10.1021/om400667t>
  • Marimuthu Thashree, Friedrich Holger B.: Microwave-Assisted Transfer Hydrogenation of Ketones by Ru(xantphos) Arene Complexes. ChemCatChem 2012, 4, 2090. <http://dx.doi.org/10.1002/cctc.201200306>
  • Alagona Giuliano, Ghio Caterina: The fate of branched and linear isomers in the rhodium-catalyzed hydroformylation of 3,4,4-trimethylpent-1-ene. Theor Chem Accounts 2012, 131, 1142. <http://dx.doi.org/10.1007/s00214-012-1142-x>
  • Farkas Gergely, Balogh Szabolcs, Madarász József, Szöllősy Áron, Darvas Ferenc, Ürge László, Gouygou Maryse, Bakos József: Phosphine–phosphite ligands: chelate ring size vs. activity and enantioselectivity relationships in asymmetric hydrogenation. Dalton Trans. 2012, 41, 9493. <http://dx.doi.org/10.1039/c2dt30386h>
  • Koblenz Tehila S., Dekker Henk L., de Koster Chris G., van Leeuwen Piet W. N. M., Reek Joost N. H.: Control of the Coordination Geometry Around Platinum by a Supramolecular Capsule. Euro J Inorg Chem 2011, 2011, 4837. <http://dx.doi.org/10.1002/ejic.201100809>
  • Bauer Gernot, Englert Cornelia, Nieger Martin, Gudat Dietrich: Different coordination behavior of a catechol phosphine and its sulfide: Formation of an unprecedented dinuclear rhodium complex with a non-coordinated PS unit. Inorg Chim Ada 2011, 374, 240. <http://dx.doi.org/10.1016/j.ica.2011.02.076>
  • Belabassi Yamina, Bravo-Altamirano Karla, Montchamp Jean-Luc: Regiocontrol in the palladium-catalyzed hydrophosphinylation of terminal alkynes. J Organomet Chem 2011, 696, 106. <http://dx.doi.org/10.1016/j.jorganchem.2010.08.018>
  • Gathy Thomas, Riant Olivier, Peeters Daniel, Leyssens Tom: A theoretical study of the electronic effect of the ligand bite angle on the hydrosilylation reaction of ketones by Cu(I) diphosphine complexes. j organometall chem 2011, 696, 3425. <http://dx.doi.org/10.1016/j.jorganchem.2011.07.041>
  • Dias Roberta P., Rocha Willian R.: DFT Study of the Homogeneous Hydroformylation of Propene Promoted by a Heterobimetallic Pt–Sn Catalyst. Organomettalics 2011, 30, 4257. <http://dx.doi.org/10.1021/om1012067>
  • Li Changxiu, Pattacini Roberto, Braunstein Pierre: A fluorene-based diphosphinite ligand, its Ni, Pd, Pt, Fe, Co and Zn complexes and the first structurally characterized diphosphinate metal chelates. Inorg Chim Ada 2010, 363, 4337. <http://dx.doi.org/10.1016/j.ica.2010.06.007>
  • Kaganovsky Luba, Gelman Dmitri, Rueck-Braun Karola: Trans-chelating ligands in palladium-catalyzed carbonylative coupling and methoxycarbonylation of aryl halides. J Organomet Chem 2010, 695, 260. <http://dx.doi.org/10.1016/j.jorganchem.2009.10.001>
  • Chikkali Samir H., Nieger Martin, Gudat Dietrich: Stoichiometry controlled self-assembly of tri- and octa-nuclear palladium–yttrium complexes. New J Chem 2010, 34, 1348. <http://dx.doi.org/10.1039/c0nj00020e>
  • Maldonado Ana G., Hageman Jos A., Mastroianni Sergio, Rothenberg Gadi: Backbone Diversity Analysis in Catalyst Design. Adv. Synth. Catal. 2009, 351, 387. <http://dx.doi.org/10.1002/adsc.200800574>
  • Chikkali Samir H., Gudat Dietrich, Lissner Falk, Niemeyer Mark, Schleid Thomas, Nieger Martin: Template-Controlled Assembly of Ditopic Catechol Phosphines: A Strategy for the Generation of Complexes of Bidentate Phosphines with Different Bite Angles. Chem. Eur. J. 2009, 15, 482. <http://dx.doi.org/10.1002/chem.200801517>
  • Koseo��lu Ahmet, Kraka Elfi, Serinda�� Osman, Varnali Tereza: Comparison of Ni, Pd, Pt complexes of N,N-bis(dialkylphosphinomethyl)aminomethane: A DFT study. Journal of Molecular Structure: THEOCHEM 2009, 896, 49. <http://dx.doi.org/10.1016/j.theochem.2008.11.001>
  • Haddow Mairi F., Middleton Ann J., Orpen A. Guy, Pringle Paul G., Papp Rainer: Stereoelectronic effects in a homologous series of bidentate cyclic phosphines. A clear correlation of hydroformylation catalyst activity with ring size. Dalton Trans 2009, 202. <http://dx.doi.org/10.1039/b815056g>
  • Aguilà David, Escribano Esther, Speed Saskia, Talancón Daniel, Yermán Luis, Alvarez Santiago: Calibrating the coordination chemistry tool chest: metrics of bi- and tridentate ligands. Dalton Trans 2009, 6610. <http://dx.doi.org/10.1039/b904938j>
  • Kaltzoglou Andreas, Fässler Thomas F., Aslanidis Paraskevas: A luminescent copper(I) bromide complex chelated with 4,5- bis (diphenylphosphano)-9,9-dimethyl-xanthene. J Coord Chem 2008, 61, 1774. <http://dx.doi.org/10.1080/00958970701656106>
  • Uchimura Hirofumi, Ito Jun-ichi, Iwasa Seiji, Nishiyama Hisao: Oxidative addition reactions and stereochemistry on rhodium/4,5-bis(2-oxazolinyl)xanthene complexes. J Organomet Chem 2007, 692, 481. <http://dx.doi.org/10.1016/j.jorganchem.2006.04.040>
  • Knowles Jonathan P., Whiting Andrew: The Heck–Mizoroki cross-coupling reaction: a mechanistic perspective. Org Biomol Chem 2007, 5, 31. <http://dx.doi.org/10.1039/b611547k>
  • Mbaiwa F. Foster, Becker C. A. L.: Chelate complexes from diphosphine substitution in pentakis(arylisocyanide)cobalt(I) complexes. J Coord Chem 2007, 60, 153. <http://dx.doi.org/10.1080/00958970600763201>
  • Hageman Jos A., Westerhuis Johan A., Frühauf Hans-Werner, Rothenberg Gadi: Design and Assembly of Virtual Homogeneous Catalyst Libraries –Towardsin silico Catalyst Optimisation. Adv Synth Catal 2006, 348, 361. <http://dx.doi.org/10.1002/adsc.200505299>
  • Fairlamb Ian J. S., Grant Stephanie, Tommasi Simona, Lynam Jason M., Bandini Marco, Dong Hao, Lin Zhenyang, Whitwood Adrian C.: Phosphinite Ligand Effects in Palladium(II)-Catalysed Cycloisomerisation of 1,6-Dienes: Bicyclo[3.2.0]heptanyl Diphosphinite (B[3.2.0]DPO) Ligands Exhibit Flexible Bite Angles, an Effect Derived from Conformational Changes (exo- orendo-Envelope) in the Bicyclic Ligand Scaffold. Adv Synth Catal 2006, 348, 2515. <http://dx.doi.org/10.1002/adsc.200600346>
  • Cox P.J., Kaltzoglou A., Aslanidis P.: Copper(I) halide chelates of the wide bite angle diphosphane xantphos: Crystal structures of [CuBr(xantphos)(dmpymtH)] and [CuI(xantphos)(imdtH2)]·CH3CN. Inorg Chim Ada 2006, 359, 3183. <http://dx.doi.org/10.1016/j.ica.2006.02.046>
  • Lee Sunwoo: 1,1′-Bis(oxazolinyl)ferrocene-based palladium catalysts: Synthesis, X-ray structures and applications in Suzuki and Heck coupling reactions. J Organomet Chem 2006, 691, 1347. <http://dx.doi.org/10.1016/j.jorganchem.2005.12.018>
  • Burello Enrico, Marion Philippe, Galland Jean-Christophe, Chamard Alex, Rothenberg Gadi: Ligand Descriptor Analysis in Nickel-Catalysed Hydrocyanation: A Combined Experimental and Theoretical Study. Adv Synth Catal 2005, 347, 803. <http://dx.doi.org/10.1002/adsc.200404363>
  • Hartinger Christian G., Nazarov Alexey A., Arion Vladimir B., Giester Gerald, Kuznetsov Maxim L., Galanski Markus, Keppler Bernhard K.: 1,1'-Bis(oxazolin-2-yl)ferrocenes: An Investigation of Their Complexation Behavior toward [Pd(η3-allyl)Cl]2. Eur J Inorg Chem 2005, 2005, 1589. <http://dx.doi.org/10.1002/ejic.200400737>
  • Nazarov Alexey A., Koroteev Mikhail P., Hartinger Christian G., Keppler Bernhard K., Nifant'ev Eduard E.: Bis- and tris-bicyclophosphites of d-glucofuranoside. Unexpected catalysis of P(III/V)-oxidation by triethylamine. Tetrahedron 2005, 61, 10943. <http://dx.doi.org/10.1016/j.tet.2005.08.102>
  • Damoense Llewellyn, Datt Michael, Green Mike, Steenkamp Casper: Recent advances in high-pressure infrared and NMR techniques for the determination of catalytically active species in rhodium- and cobalt-catalysed hydroformylation reactions. Coord Chem Rev - 2004, 248, 2393. <http://dx.doi.org/10.1016/j.ccr.2004.04.005>
  • Petöcz György, Berente Zoltán, Kégl Tamás, Kollár László: Xantphos as cis- and trans-chelating ligand in square-planar platinum(II) complexes. Hydroformylation of styrene with platinum–xantphos–tin(II)chloride system. J Organomet Chem 2004, 689, 1188. <http://dx.doi.org/10.1016/j.jorganchem.2003.10.045>
  • Meijer R.H, Ligthart G.B.W.L, Meuldijk J, Vekemans J.A.J.M, Hulshof L.A, Mills A.M, Kooijman H, Spek A.L: Triruthenium dodecacarbonyl/triphenylphosphine catalyzed dehydrogenation of primary and secondary alcohols. Tetrahedron 2004, 60, 1065. <http://dx.doi.org/10.1016/j.tet.2003.11.082>
  • Deprèle Sylvine, Montchamp Jean-Luc: Environmentally Benign Synthesis of H-Phosphinic Acids Using a Water-Tolerant, Recyclable Polymer-Supported Catalyst. Org Lett 2004, 6, 3805. <http://dx.doi.org/10.1021/ol0484198>
  • Izubiri Mireia Rodriguez, Slawin Alexandra M. Z., Cole-Hamilton David, Woollins J. Derek: Synthesis of New Phosphino-Amines, their Metal Complexes and their Application in Catalysis. Phosphorus Sulfur Silicon Relat Elem 2001, 169, 117. <http://dx.doi.org/10.1080/10426500108546604>