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2019 | 126 | 36-64
Article title

Ionic liquid assisted olefin reactions

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Abstracts
EN
In this review article the authors studied the ionic liquid assisted various alkene reactions with various metal complex catalysts such as Isomerization, Hydrogenation, Hydroformylation, Metathesis-Oligomerization, Dimerization, Arylation, Cyclization, Polymerization, Epoxidation, Michael addition and Tandem Cross-coupling reactions.
Year
Volume
126
Pages
36-64
Physical description
Contributors
  • Department of Chemistry, Annamalai University, Annamalainagar - 608002, India
author
  • Department of Chemistry, M. R. Gov. Arts College, Mannargudi, Tamilnadu - 614 001, India
  • Department of Chemistry, Sourashtra College, Madurai - 625 004, India
References
  • [1] S. Ming-bo, L. Gui-yan, Z. Jing-jing, W. Xiao-yu, W. Jian-hui, Chem. Res. Chin. Univ. 28 (2012) 67-69
  • [2] H. Olivier-Bourbigou, L. Magna, D. Morvan, Appl. Catal. A, 373 (2010) 1-4
  • [3] M. Setty-Fichman, J. Blum, Y. Sasson, M. Eisen, Tetrahedron Lett. 35(5), (1994) 781-788
  • [4] R. Bujok, M. Bieniek, M. Masnyk, A. Michrowska, A. Sarosiek, H. Stępowska, D. Arlt, K. Grela, J. Org. Chem., 69(20) (2004) 6894-6899
  • [5] S. Lentini, P. Galloni, I. Garcia-Bosch, M. Costas, V. Conte, Inorg. Chem. Acta. 410 (2014) 60-64
  • [6] K. Funabiki, T. Komeda, Y. Kubota, M. Matsui, Tetrahedron. 65 (2009) 7457-7463.
  • [7] N. T. S. Phan, M. Van Der Sluys, C.W. Jones, C. W. Adv. Synth. Catal 348(6) (2006) 609-679
  • [8] P. Migowski, J. Dupont, Chem. Eur. J. 13 (2007) 32-39
  • [9] Y. L. Gu, G. X. Li, Adv. Synth. Catal., 315 (2009) 817-847
  • [10] G. Parshall, J. Am. Chem. Soc. 94 (1972) 8716-8720
  • [11] J.F. Knifton, J. Mol. Catal. A: Chem. 43(1) (1987) 65-78
  • [12] L. Magna, S. Harry, A. Faraj, H. Olivier-Bourbigou, Oil & Gas Sci. Tech. – Rev. IFP Energies nouvelles, 68 (2013) 415-428
  • [13] M. Koy, H. J. Altmann, B. Autenrieth, W. Frey, M. R. Buchmeiser, Beilstein J. Org. Chem. 11 (2015) 1632-1638
  • [14] A. T. Priya, B. B. Marvey, Molecules 2016, 21, 184
  • [15] C. Thurier, C. Fischmeister, C. Bruneau, H. Olivier-Bourbigou, P. H. Dixneuf, J. Mol. Catal. A Chem. 268 (2007) 127-133
  • [16] N. Audic, H. Clavier, M. Mauduit, J. C. Guillemin, J. Am. Chem. Soc. 125 (2003), 9248-9249
  • [17] C. Feher, R. Skoda foldes, E. Krivan, J. Honscok, Hungeriyan J. Ind. Chem. 39 (2011) 63-66
  • [18] M. P. Atkins, K. R. Seddon, M. Swadźba-Kwaśny, Pure Appl. Chem. 83 (2011) 1391-1406
  • [19] Y. Chauvin, H. Olivier, C. N. Wyrvalski, et al., J. Catal. 165 (1997) 275-283
  • [20] G. J. C. Mamantov, T. D. J. Dunstan, US Patent No. 5,552,241 (1996).
  • [21] R. S. Varma, V. V. Namboodiri, Chem. Commun., (2001)643-646.
  • [22] Y. Chauvin, H. Olivier-Bourbigou, Chemtech. (1995) 26-29
  • [23] Y. Chauvin, B. Gilbert, I. Guibard, J. Chem. Soc., Chem. Commun., (1990)1715-1721
  • [24] Y. Chauvin, S. Einloft, H. Olivier, Ind. Eng. Chem. Res. 34, (1995)1149-1154
  • [25] F. A. Nasirov, F. M. Novruzova, A. M. Aslanbeili, A. G. Azizov, Petro. Chem. 47 (2007) 309-317
  • [26] S. Cacchi, G. Fabrizi, F. Gavazza, A. Goggiamani, Org. Lett. 5 (2003) 289-294
  • [27] E. Mizushima, K. Sato, T. Hayashi, M. Tanaka, Angew. Chem. Int. Ed. 41 (2002) 4563-4568
  • [28] F. Duris, D. Barbier-Baudry, A. Dormond, J. R. Desmurs, J. M. Bernard, J. Mol. Catal. A: Chem. 188 (2002) 97-103
  • [29] J. Kaur, K. Griffin, B. Harrison, I. V. Kozhevnikov, J. Catal. 208 (2002) 448
  • [30] C. G. Frost, K.Wadsworth, J. Chem. Commun. (2001) 2316
  • [31] J. Mo, L. Xu, J. Xiao, J. Am. Chem. Sco. 127 (2005) 751-760
  • [32] A. G. Avent, P. A. Chaloner, M. P. Day, K. R. Seddon, T. J. Welton, Chem. Soc. Dalton Trans. (1994) 3405-3410
  • [33] P. Kölle, R. Dronskowski, Inorg. Chem. 43 (2004) 2803-2809
  • [34] K. S. A. Vallin, P. Emilsson, M. Larhed, A. Hallberg, J. Org. Chem. 67 (2002) 6243-6247
  • [35] K. S. A. Vallin, M. Larhed, A. Hallberg, J. Org. Chem. 66 (2001) 4340-4348
  • [36] S. Chandrasekhar, C. Narsihmulu, S. S. Sultana, N. R. Reddy, Org. Lett. 4 (2002) 4399-4404
  • [37] M. J. Burk, Y. M. Wang, J. R. Lee, J. Am. Chem. Soc. 118 (1996) 5142-1546
  • [38] W. Cabri, I. Candiani, A. Bedeschi, J. Org. Chem. 58 (1993) 7421-7426
  • [39] K. S. A. Vallin, Q. Zhang, M. Larhed, D. P. Curran, A. Hallberg, J. Org. Chem. 68 (2003) 6639-6642
  • [40] C. G. Hartung, K. Köhler, M. Beller, Org. Lett. 1 (1999) 709-711
  • [41] M. M. S. Andappan, P. Nilsson, H. von Schenck, M. Larhed, J. Org. Chem. 69 (2004) 5212-5217
  • [42] J. M. Brown, J.J. Perez-Torrente, N. W. Alcock, H. Clase, J. Organometallics 14 (1995) 207-213
  • [43] R. R. Deshmukh, R. Rajagopal, K. V. Srinivasan, Chem. Commun. (2001) 5544-1545
  • [44] D. B. Zhao, Z. F. Fei, T. J. Geldbach, R. Scopelliti, P. J. Dyson, J. Am. Chem. Sco. 126(48) (2004) 15876-15882
  • [45] C. Chiappe, D. Pieraccini, D. B. Zhao, Z. F. Fei, P. J. Dyson, Adv. Synth. Catal. 348(1-2) (2006) 68-74
  • [46] Z. F Fei, D. B. Zhao, D. Pieraccini, W. H. Ang, T. J. Geldbach, R. Scopelliti, C. Chiappe, P. J. Dyson, Organometallics, 26(7) (2007) 1588-1598
  • [47] V. Calo, A. Nacci, A. Monopoli, A. E. Ieva, N. Cioffi, Org. Lett. 7(4) (2005) 617-620.
  • [48] V. Calo, A. Nacci, A. Monopoli, F. Montingelli, J. Org. Chem. 70(15) (2005)
  • [49] Y. G. Cui, I. Biondi, M. Chaubey, X. Yang, Z. F. Fei, R. Scopelliti, C. G. Hartinger, Y. Li, C. Chiappe, P. J. Dyson, Phys. Chem. Chem. Phys. 12(8) (2010) 1834-1841
  • [50] S. Y. Gao, H. J. Zhang, X. M. Wang, W. P. Mai, C. Y. Peng, L. H. Ge. Nanotec. 16(8) (2005) 1234-1237
  • [51] A. Corma, H. Garcia, A. Leyva, J. Mol. Catal. A. Chem. 230 (2005) 97-105
  • [52] A. Corma, H. Garcia, A. Leyva, Tetrahedron, 61(41) (2005) 9848-9854
  • [53] S. R. Dubbaka, D. B. Zhao, Z. F. Fei, C. M. R. Volla, P. J. Dyson, P. Vogel, Synlett,(18) (2006) 3155-3157
  • [54] K. Qiao, Y. Deng, Tetrahedron Lett. 44 (2003) 2191-2193
  • [55] J. D. Holbrey, K. H. Shaughnessy, M. A. Klingshirn, G. A. Broker, R. D. Rogers, Transition metal catalyzed co/olefin co-polymerization in room temperature ionic liquids.-Web Ref.2018.
  • [56] G. Liu, X. Liu, M. Gagliardo, D.J. Beetstra, A. Meetsma, B. Hessen, Organometallics 27 (2008) 2316-2320
  • [57] S. Liu, J. Xiao, J. Mol. Catal., A: Chem. 270 (2007) 1
  • [58] a) H. Adolfsson, in Modern Oxidation Methods, (Ed. J. E. Bäckvall), Wiley- VCH, Weinheim, Germany, 2004, 21-49
  • b) Q.-H. Xia, H.-Q. Ge, C.-P. Ye, Z.- M. Liu, K.-X. Su, Chem. Rev. 105 (2005) 1603-1662
  • c) F.E. Kühn, J. Zhao, W.A. Herrmann, Tetrahedron: Asymmetry, 16 (2005) 3469-3479
  • d) R.A. Sheldon, in Applied Homogeneous Catalysis with Organometallic Compounds, (Eds. B. Cornils, W.A. Herrmann) Wiley-VCH, Weinheim, Germany, 2nd Edn., 2002, 412-426
  • e). Daniel Betz, Alexander Raith, Mirza Cokoja, Fritz E. Kühn, Chem Sus Chem, 3 (2010) 559-562
  • [59] a) H. B. Kagan, H. Mimoun, C. Marc, V. Schurig, Angew. Chem. Int. Ed. Engl. 18 (1979) 485-486
  • b) T. Katsuki, K.B. Sharpless, J. Am. Chem. Soc. 102 (1980), 5974-5976
  • c) I.D. Williams, S.F. Pederson, K.B. Sharpless, S.J. Lippard, J. Am. Chem. Soc. 106 (1984), 6430-6431
  • d) M. Palucki, P.J. Pospisil, W. Zhang, E.N. Jacobsen, J. Am. Chem. Soc. 116 (1994) 9333-9334
  • e) P. Pietikäinen, Tetrahedron, 54 (1998) 4319-4326
  • f) N. Makita, Y. Hoshino, H. Yamamoto, Angew. Chem. Int. Ed. Engl. 42 (2003) 941-943
  • g) W. Zhang, A. Basak, Y. Kosugi, Y. Hoshino, H. Yamamoto, Angew. Chem. Int. Ed. Engl. 44 (2005) 4389-4391
  • h) Z. Bourhani, A.V. Malkov, Chem. Commun. 2005, 4592-4595
  • i) F.E. Kühn, A.M. Santos, M. Abrantes, Chem. Rev. 106 (2006) 2455-2457
  • j) W.A. Herrmann, F.E. Kühn, Acc. Chem. Res. 30(1997) 169-180
  • k) F.E. Kühn, A. Scherbaum, W.A. Herrmann, J. Organomet. Chem. 689 (2004) 4149-4164
  • l) F.E. Kühn, A.M. Santos, W.A. Herrmann, Dalton Trans. 15 (2005), 2483-2491.
  • [60] a) S. Bellemin-Laponnaz, K.S. Coleman, J.A. Osborn, Polyhedron 18(1999) 2533-2536
  • b) A. Berkessel, P. Kaiser, J. Lex, Chem.-Eur. J. 9(2003) 4746-4756
  • c) C.E. Tucker, K.G. Davenport, Hoechst Celanese Corporation, US Patent 5618958, 1997
  • d) M.J. Sabater, M.E. Domint, A. Corma, J. Catal. 2002, Chapter VII 180 210, 192-197
  • e) R.J. Cross, P.D. Newman, R.D. Peacock, D. Stirling, J. Mol.Catal. A: Chem. 144 (1999) 273-284
  • f) A.A. Valente, I.S. Gonçalves, A.D. Lopes, J.E. Rodríguez-Borges, M. Pillinger, C.C. Romão, J. Rocha, X. García- Mera, New J. Chem. 25(2001) 959-964
  • g) S.M. Bruno, S.S. Balula, A.A. Valente, F.A. Almeida Paz, M. Pillinger, C. Sousa, J. Klinowski, C. Freire, P. Ribeiro-Claro, I.S. Goncalves, J. Mol. Cat. A: Chem. 270 (2007) 185-194
  • h) Y. Wang, Z. Wu, Z. Li, X.-G. Zhou, Tetrahedron Lett. 50 (2009) 2509-2511
  • i) K.R. Jain, W.A. Herrmann, F.E. Kühn, Coord. Chem. Rev. 252 (2008) 556-568
  • [61] a) P. Neves, S. Gago, C.C.L. Pereira, A.D. Lopes, I.S. Gonçalves, M. Pillinger, C.M. Silva, A.A. Valente, Catal. Lett. 132 (2009) 94-103
  • b) B. Monteiro, S. Gago, P. Neves, A.A. Valente, I.S. Gonçalves, C.C.L. Pereira, C.M. Silva, M. Pillinger, Catal. Lett. 129 (2009), 350-357
  • c) A. Günyar, M.D. Zhou, M. Drees, P.N.W. Baxter, G. Bassioni, E. Herdtweck, F.E. Kühn, Dalton Trans. 40 (2009) 8746-8754
  • d) A.M. Al-Ajlouni, A. Günyar, M.D. Zhou, P.N.W. Baxter, F.E. Kühn, Eur. J. Inorg. Chem.8 (2009) 1019-1026
  • e) P.J. Costa, M.J. Calhorda, F.E. Kühn, Organometallics, 29 (2010) 303-311
  • [62] J. Zhao, A.M. Santos, E. Herdtweck, F.E. Kühn, J. Mol. Catal. A: Chem. 222 (2004) 265-271
  • [63] a) F. Amor, P. Royo, T.P. Spaniol, J. Okuda, J. Organomet. Chem. 604(2000) 604, 126-131
  • b) A. Barretta, F.G.N. Cloke, A. Feigenbaum, M.L.H. Green, A. Gourdon, K. Prout, J. Chem. Soc. Chem. Commun. (1981) 156-158
  • c) A. Barretta, K.S. Chong, F.G.N. Cloke, A. Feigenbaum, M.L.H. Green, J. Chem. Soc, Dalton Trans. (1983) 861–864
  • d) J. Zhao, E. Herdtweck, F.E. Kühn, J.Organomet. Chem. 691 (2006) 2199-2206
  • e) J. Zhao, K.R. Jain, E. Herdtweck, F.E. Kühn, Dalton Trans. (2007) 5567-5571
  • f) A. Capapé, A. Raith, F.E. Kühn, Adv. Synth. Catal. 351(2009) 66-70.
  • [64] a) P. Eilbracht, Chem. Ber. 109 (1976) 1429-1435
  • b) P. Eilbracht, J. Organomet. Chem. 1976, 120, C37-C38
  • c) P. Eilbracht, J. Organomet. Chem. 127(1977) C48-C50
  • d) P. Eilbracht, P. Dahler, U. Mayser, E. Henkes, Chem. Ber. 113 (1980) 1033-1046
  • [65] a) G. Liu, X. Liu, M. Gagliardo, D.J. Beetstra, A. Meetsma, B. Hessen, Organometallics, 27 (2008) 2316-2320
  • b) A. Doppiu, U. Englert, A. Salzer, Inorg. Chim. Acta, 350 (2003) 435-441
  • c) S. Ciruelos, A. Doppiu, U. Englert, A. Salzer, J. Organomet. Chem. 663 (2002) 183-191
  • d) H. Wang, G. Kehr, R. Chapter VII 181 Fröhlich, G. Erker, Angew. Chem. Int. Ed. Engl. 45(2007) 4905-4908
  • e) S. Gómez-Ruiz, D. Polo-Cerón, S. Prashar, M. Fajardo, V.L. Cruz, J. Ramos, E. Hey-Hawkins, J. Organomet. Chem. 693 (2008) 601-610
  • f) J. Honzíček, F.A. Almeida Paz, C.C. Romão, Eur. J. Inorg. Chem. (2007) 2827-2838
  • [66] a) S. Ciruelos, U. Englert, A. Salzer, Organometallics 19 (2000) 2240-2242
  • b) K.B. Wiberg, K.A. Saegebarth, J. Am. Chem. Soc. 79 (1957) 2822-2824
  • c) N.L. Armanasco, M.V. Baker, M.R. North, B.W. Skelton, A.H. White, J. Chem. Soc. Dalton Trans., (1998) 1145-1149
  • d) M.V. Baker, M.R. North, J. Organomet. Chem. 565(1998) 225-230
  • e) C.E. Zybill, in Synthetic Methods of Organometallic and Inorganic Chemistry (Ed. W.A. Herrmann), Georg Thieme Verlag: Stuttgart – New York, 1997, Vol. 8, p. 103.
  • [67] J.G. Huddleston, A.E. Visser, W.M. Reichert, H.D. Willauer, G.A. Broker, R.D. Rogers, Green Chem. 3(2001) 156-164
  • [68] a) A.E. Visser, R.P. Swaloski, R.D. Rogers, Green Chem. 2 (2000) 1-4
  • b) J.G. Huddleston, H.D. Willauer, R.P. Swaloski, A.E. Visser, R. D. Rogers, Chem. Commun. (1998) 1765-1766
  • [69] a) T. Welton, Chem. Rev. 99 (1999) 2071-2083
  • b) A. Riisager, R. Fehrmann, M. Haumann, P. Wasserscheid, Eur. J. Inorg. Chem. (2006) 695-706
  • c) R. Giernoth, Top. Curr. Chem. 276(2007) 1-23
  • [70] C.E. Song, E.J. Roh, Chem. Commun. 10 (2000) 837-838
  • [71] a) K. Srinivas, A. Kunar, S. Chauhan, Chem. Commun. 20 (2002) 2456-2457
  • b) Z. Li, C. Xia, Tetrahedron Lett. 44 (2003) 2069-2071
  • c) Z. Li, C. Xia, M. Ji, Appl. Catal., A 252(2003) 17-21
  • d) J. Dupont, R. Souza, P. Suarez, Chem. Rev. 102(2002) 3667-3692
  • e) R. Saladino, R. Bernini, V. Neri, C. Crestini, Appl. Catal., A 360(2009) 171-176
  • f) A. Valente, Ž. Petrovski, L.C. Branco, C.A.M. Afonso, M. Pillinger, A.D. Lopes, C.C. Romão, C.D. Nuñes, I.S. Gonçalves, J. Mol. Catal. A: Chem. 218 (2004) 5-11
  • g) F.E. Kühn, J. Zhao, M. Abrantes, W. Sun, C. Afonso, L. Branco, I.S. Gonçalves, M. Pillinger, C.C. Romão, Tetrahedron Lett. 46 (2005) 47-52
  • h) M. Herbert, A. Galindo, F. Montilla, Catal. Comm. 8(2007) 987-990
  • i) C. Bibal, J.C. Daran, S. Deroover, R. Poli, Polyhedron 2010, 29, 639-647
  • j) K.R. Jain, F.E. Kühn, Dalton Trans. 17 (2008) 2221-2227
  • [72] D. Betz, W.A. Herrmann, F.E. Kühn, J. Organomet. Chem. 20 (2009) 3320-3324
  • [73] Alev Günyar, Daniel Betz, Markus Drees, Eberhard Herdtweck, Fritz E. Kühn, J. Mol. Catal. A: Chem. 331 (2010) 117-124
  • [74] a) F.E. Kühn, E. Herdtweck, J.J. Haider, W.A. Herrmann, I.S. Gonçalves, A.D. Lopes, C.C. Romão, J. Organomet. Chem. 1999, 583, 3
  • b) F.E. Kühn, A.D. Lopes, A.M. Santos, E. Herdtweck, J.J. Haider, C.C. Romão, A.G. Santos, J. Mol. Catal. A: Chem. 2000, 151, 147
  • c) F.E. Kühn, A.M. Santos, A.D. Lopes, I.S. Gonçalves, E. Herdtweck, C.C. Romão, J. Mol. Catal. A: Chem. 2000, 164, 25
  • d) F.E. Kühn, A.M. Santos, I.S. Gonçalves, C.C. Romão, A.D. Lopes, Appl. Organomet. Chem. 2001, 15, 43
  • e) S. Gago, P. Neves, B. Monteiro, M. Pessêgo, A.D. Lopes, A.A. Valente, F.A. Almeida Paz, M. Pillinger, J. Moreira, C.M. Silva, I.S. Gonçalves, Eur. J. Inorg. Chem. 2009, 4528
  • f) L.F. Veiros, A. Prazeres, P.J. Costa, C.C. Romão, F.E. Kühn, M.J. Calhorda, Dalton Trans.2006, 1383
  • g) M. Groarke, I.S. Gonçalves, W.A. Herrmann, F.E. Kühn, J. Organomet. Chem. 2002, 649, 108.
  • [75] F.E. Kühn, M. Groarke, É. Bencze, E. Herdtweck, A. Prazeres, A.M. Santos, M.J. Calhorda, C.C. Romão, I.S. Gonçalves, A.D. Lopes, M. Pillinger, Chem.-Eur. J. 2002, 8, 2370.
  • [76] J.G. Huddleston, A.E. Visser, W.M. Reichert, H.D. Willauer, G.A. Broker, R.D. Rogers, Green Chem. 2001, 3, 156
  • [77] Daniel Betz, Fritz E. Kühn, in: e-Eros (Encyclopedia of Reagents for Organic Synthesis, L. A. Parquette (ed.), Wiley-VCH, 2010, 1-8.
  • [78] a) J. Rudolf, K.L. Reddy, J.P. Chiang, K.B. Sharpless, J. Am. Chem. Soc. 1997, 119, 6189
  • b) W.A. Herrmann, R.M. Kratzer, H. Ding, W.R. Thiel, H. Glas, J. Organomet. Chem. 1998, 555, 293
  • c) H. Adolfsson, C. Coperet, J.P. Chiang, A.K. Yudin, J. Org. Chem. 2000, 65, 8651
  • d) H. Adolfsson, A. Converso, K.B. Sharpless, Tetrahedron Lett. 1999, 40, 3991
  • e) W.A. Herrmann, H. Ding, R.M. Kratzer, F.E. Kühn, J.J. Haider, R.W. Fischer, J. Organomet. Chem. 1997, 549, 319
  • f) H. Rudler, J.R. Gregorio, B. Denise, J.M. Bregeault, A. Deloffre, J. Mol. Catal. A: Chem. 1998, 133, 255.
  • [79] a) F.E. Kühn, A.M. Santos, P.W. Roesky, E. Herdtweck, W. Scherer, P. Gisdakis, I.V. Yudanov, C. di Valentin, N. Rösch, Chem. Eur. J. 1999, 5, 3603
  • b) P. Ferreira, W.M. Xue, E. Bencze, E. Herdtweck, F.E. Kühn, Inorg. Chem. 2001, 40, 5834
  • c) A.M. Santos, F.E. Kühn, K. Bruus-Jensen, I. Lucas, C.C. Romão, E. Herdtweck, J. Chem. Soc. Dalton Trans. 2001, 1332
  • d) J. Mink, G. Keresztury, A. Stirling, W.A. Herrmann, Spectrochim. Acta Part A 1994, 50, 2039.
  • [80] a) J.H. Espenson, W.-D. Wang, J. Am. Chem. Soc. 1998, 120, 11335
  • b) M. Nakajima, Y. Sasaki, H. Iwamoto, S. Hashimoto, Tetrahedron Lett. 1998, 39, 87
  • c) C.D. Nuñes, M. Pillinger, A.A. Valente, I.S. Gonçalves, J. Rocha, P. Ferreira, F.E. Kühn, Eur. J. Inorg. Chem. 2002, 1100
  • d) M.J. Sabater, M.E. Domine, A. Corma, J. Catal. 2002, 210, 192
  • e) E. Da Palma Carreiro, A.J. Burke, M.J. Marcelo Curto, A.J. Teixeira, J. Mol. Catal. A: Chem. 2004, 217, 69
  • f) K. Shimura, K. Fujita, H. Kanai, K. Utani, S. Imamura, Appl. Catal. A 2004, 274, 253
  • g) S.M. Nabavizadeh, Dalton Trans. 2005, 1644
  • h) S.M. Nabavizadeh, A. Akbari, M. Rashidi, Eur. J. Inorg. Chem. 2005, 2368;
  • i) S.M. Nabavizadeh, A. Akbari, M. Rashidi, Dalton Trans. 2005, 2423.
  • [81] W.A. Herrmann, J.D.G. Correia, M.U. Rauch, G.R.J. Artus, F.E. Kühn, J. Mol. Catal. A: Chem. 1997, 118, 33
  • [82] a) P.D. Benny, J.L. Green, H.P. Engelbrecht, C.L. Barnes, S.S. Jurisson, Inorg. Chem. 2005, 44, 2381
  • b) Z.-K. Li, Y. Li, L. Lei, C.-M. Che, X.-G. Zhou, Inorg. Chem. Commun. 2005, 8, 307;
  • c) W.A. Herrmann, M.U. Rauch, G.R.J. Artus, J. Inorg. Chem. 1996, 35, 1988
  • d) F.E. Kühn, M.U. Rauch, G.M. Lobmaier, G.R.J. Artus, W.A. Herrmann, Chem. Ber./Recueil 1997, 130, 1427.
  • [83] a) M.D. Zhou, J. Zhao, J. Li, S. Yue, C.N. Bao, J. Mink, S.L. Zang, F.E. Kühn, Chem. Eur. J. 2007, 13, 158
  • b) M.D. Zhou, S.L. Zang, E. Herdtweck, F.E. Kühn, J. Organomet. Chem. 2008, 693, 2473
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bwmeta1.element.psjd-c7c9ec7c-a475-4fb8-820e-d9bc6b54aa9c
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