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化学进展 2013, Vol. 25 Issue (0203): 330-339 DOI: 10.7536/PC120746 前一篇   后一篇

• 综述与评论 •

异核多金属N-杂环卡宾化合物的合成及应用

顾绍金*1,2, 徐卫林1,2, 黄菁菁2   

  1. 1. 武汉纺织大学材料科学与工程学院 武汉 430073;
    2. 新型纺织材料绿色加工及其 功能化教育部重点实验室 武汉 430073
  • 收稿日期:2012-07-01 修回日期:2012-10-01 出版日期:2013-02-24 发布日期:2012-12-28
  • 通讯作者: 顾绍金 E-mail:gushaojin2005@163.com
  • 基金资助:

    国家重点基础研究发展计划(973)项目(No.2012CB722701)和国家自然科学基金项目(No.21202127)资助

Synthesis and Applications of Heteromultimetallic Complexes Containing N-Heterocyclic Carbenes

Gu Shaojin*1,2, Xu Weilin1,2, Huang Jingjing2   

  1. 1. School of Materials Science and Engineering, Wuhan Textile University, Wuhan 430073, China;
    2. Key Laboratory of Green Processing and Functional Textiles of New Textile Materials, Ministry of Education, Wuhan Textile University, Wuhan 430073, China
  • Received:2012-07-01 Revised:2012-10-01 Online:2013-02-24 Published:2012-12-28

以N-杂环卡宾为配体的异核多金属化合物的合成、物理化学性质以及应用取得了很大的发展,尤其在多步串联催化反应方面显示出了优越的催化活性。本文根据构建异核多金属的配体种类,对异核多金属N-杂环卡宾化合物的合成及其应用进行了分类总结,并对异核多金属N-杂环卡宾化合物未来的研究前景进行了展望。

Due to the strong electronic donor properties and the versatile structures which can be readily modified, as well as the distinct topography, N-heterocyclic carbene(NHC)is a new class of ligands as an alternative to traditional phosphine ones. The catalytic properties of NHC-metal (NHC-M) complexes in homogeneous and asymmetric catalysis have been a focused research field and many successful results have been reported in recent years. The synthesis strategies, physical and chemical properties, as well as applications of heteromultimetallic complexes based on N-heterocyclic carbene ligand have made great development. It is worth noting that the remarkable catalytic activities have been obtained in multi-step catalytic tandem reaction. In this paper, the synthesis and applications of heteromultimetallic complexes containing N-heterocyclic carbene are summarized and reviewed according to the type of N-heterocyclic carbene ligand. The type of N-heterocyclic carbene ligand include:(a) heteromultimetallic complexes based on a triazolyl-di-ylidene ligand; (b) heteromultimetallic complexes based on a bridged bis(imidazol-2-ylidene) ligand; (c) heteromultimetallic complexes based on a functionalized multidentate N-heterocyclic ligand. Contents
1 Introduction
2 Synthesis and applications of heteromultimetallic complexes containing N-heterocyclic carbene
2.1 Heteromultimetallic complexes based on a triazolyl-di-ylidene ligand
2.2 Heteromultimetallic complexes based on a bridged bis(imidazol-2-ylidene) ligand
2.3 Heteromultimetallic complexes based on a functionalized multidentate N-heterocyclic ligand
3 Conclusion and Outlook

中图分类号: 

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[1] Arduengo A J, Harlow R L, Kline M. J. Am. Chem. Soc., 1991, 113: 361-363
[2] Garrison J C, Youngs W J. Chem. Rev., 2005, 105: 3978-4008
[3] Hahn F E, Jahnke M C. Angew. Chem. Int. Ed., 2008, 47: 3122-3172
[4] Herrmann W A. Angew. Chem. Int. Ed., 2002, 41: 1290-1309
[5] Herrmann W A, Öfele K, von Preysing D, Schneider S K. J. Organomet. Chem., 2003, 687: 229-248
[6] Lin J C Y, Huang R T W, Lee C S, Bhattacharyya A, Hwang W S, Lin I J B. Chem. Rev., 2009, 109: 3561-3598
[7] Liu Q X, Wang H, Zhao X J, Yao Z Q, Wang Z Q, Chen A H, Wang X G. CrystEngComm, 2012, 14: 5330-5348
[8] Liu Q X, Li S J, Zhao X J, Zang Y, Song H B, Guo J H, Wang X G. Eur. J. Inorg. Chem., 2010, (6): 983-988
[9] 姜岚(Jiang L), 李争宁(Li Z N), 赵德峰(Zhao D F). 化学进展(Progress in Chemistry), 2009, 21(6): 1229-1240
[10] 刘波(Liu B), 张娜(Zhang N), 陈万芝(Chen W Z). 化学进展(Progress in Chemistry), 2010, 22(11): 2134-2146
[11] Herrmann W A, Elison M, Fischer J, Köcher C, Artus G R J. Angew. Chem. Int. Ed., 1995, 34: 2371-2374
[12] Kong Y, Ren H P, Xu S S, Song H B, Liu B Y, Wang B Q. Organometallics, 2009, 28: 5934-5940
[13] Ihara E, Ishiguro Y, Yoshida N, Hiraren T, Itoh T, Inoue K. Macromolecules, 2009, 42: 8608-8610
[14] Wang X, Jin G X. Chem.-Eur. J., 2005, 11: 5758-5764
[15] Sinha A, Rahaman S M W, Sarkar M, Saha B, Daw P, Bera J K. Inorg. Chem., 2009, 48: 11114-11122
[16] Cheng Y, Sun J F, Yang H L, Xu H J, Li Y Z, Chen X T, Xue Z L. Organometallics, 2009, 28: 819-823
[17] Zeng F L, Yu Z K. Organometallics. 2008, 27: 6025-6028
[18] Sun J F, Chen F, Dougan B A, Xu H J, Cheng Y, Li Y Z, Chen X T, Xue Z L. J. Organomet. Chem., 2009, 694: 2096-2105
[19] Lu C, Gu S, Chen W, Qiu H. Dalton Trans., 2010, 39: 4198-4204
[20] Chianese A R, Bremer P T, Wong C, Reynes R J. Organometallics. 2009, 28: 5244-5252
[21] Malik H A, Sormunen G J, Montgomery J. J. Am. Chem. Soc., 2010, 132: 6304-6305
[22] Diez-Gonzalez S, Correa A, Cavallo L, Nolan S P. Chem.-Eur. J., 2006, 12: 7558-7564
[23] Marion N, Nolan S P. Acc. Chem. Res., 2008, 41: 1440-1449
[24] Wei W, Qin Y, Luo M, Xia P, Wong M S. Organometallics, 2008, 27: 2268-2272
[25] Kantchev E A B, O’Brien C J, Organ M G. Angew. Chem. Int. Ed., 2007, 46: 2768-2813
[26] Sanford M S, Love J A, Grubbs R H. Organometallics, 2001, 20: 5314-5318
[27] Gu S, Chen W. Organometallics, 2009, 28: 909-914
[28] Gu S J, Xu H, Zhang N, Chen W Z. Chem. Asian J., 2010, 5: 1677-1686
[29] Gu S, Huang J, Liu X, Liu H, Zhou Y, Xu W. Inorg. Chem. Commun., 2012, 21: 168-172
[30] Normand A T, Cavell K J. Eur. J. Inorg. Chem., 2008, 2781-2800
[31] Peris E, Crabtree R H. Coord. Chem. Rev., 2004, 248: 2239-2246
[32] Poyatos M, Mata J A, Peris E. Chem. Rev., 2009, 109: 3677-3707
[33] Pugh D, Danopoulos A A. Coord. Chem. Rev., 2007, 251: 610-641
[34] Gu S, Chen C, Qiu H, Chen W. Curr. Org. Chem., 2011, 15: 3291-3308
[35] Gu S, Ni P, Chen W. Chin. J. Catal., 2010, 31: 875-886
[36] 白赢(Bai Y), 彭家建(Peng J J), 胡应乾(Hu Y Q), 厉嘉云(Li J Y), 来国桥(Lai G Q), 蒋剑雄(Jiang J X). 化学进展(Progress in Chemistry), 2009, 21(12): 2613-2624
[37] Mas-Marzá E, Mata J A, Peris E. Angew. Chem. Int. Ed., 2007, 46: 3729-3731
[38] Zanardi A, Corbern R, Mata J A, Peris E. Organometallics, 2008, 27: 3570-3576
[39] Zanardi A, Mata J A, Peris E. J. Am. Chem. Soc., 2009, 131: 14531-14537
[40] Zanardi A, Mata J A, Peris E. Chem. Eur. J., 2010, 16: 10502-10506
[41] Zanardi A, Mata J A, Peris E. Chem. Eur. J., 2010, 16: 13109-13115
[42] Sabater S, Mata J A, Peris E. Chem. Eur. J., 2012, 18: 6380-6385
[43] Raynal M, Cazin C S J, Vallee C, Olivier-Bourbigou H, Braunstein P. Dalton Trans., 2009, 3824-3832
[44] Zamora M T, Ferguson M J, McDonald R, Cowie M. Dalton Trans., 2009, 7269-7287
[45] Catalano V J, Malwitz M A, Etogo A O. Inorg. Chem., 2004, 43: 5714-5724
[46] Ghosh A K, Catalano V J. Eur. J. Inorg. Chem., 2009, 1832-1843
[47] Catalano V J, Moore A L, Shearer J, Kim J. Inorg. Chem., 2009, 48: 11362-11375
[48] Strasser C E, Catalano V J. J. Am. Chem. Soc., 2010, 132: 10009-10011
[49] Strasser C E, Catalano V J. Inorg. Chem., 2011, 50: 11228-11234
[50] Dyson G, Frison J C, Simonovic S, Whitwood A C, Douthwaite R E. Organometallics, 2008, 27: 281-288
[51] Zhong R, Wang Y N, Guo X Q, Chen Z X, Hou X F. Chem. Eur. J., 2011, 17: 11041-11051
[52] Gu S, Xu D, Chen W. Dalton Trans., 2011, 40: 1576-1583
[53] Gu S, Liu B, Chen J, Wu H, Chen W. Dalton Trans., 2012, 41: 962-970
[54] Arnold P L, Liddle S T. Organometallics, 2006, 25: 1485-1491
[55] 陈超(Chen C), 邱化玉(Qiu H Y), 刘爱玲(Liu A L), 陈丹(Chen D), 汤谷平(Tang G P), 陈万芝(Chen W Z). 无机化学学报(Chinese Journalof Inorganic Chemistry), 2011, 21: 1423-1430
[56] Wimberg J, Meyer S, Dechert S, Meyer F. Organometallics, 2012, DOI: 10.1021/om300335w
[57] Mendoza-Espinosa D, Donnadieu B, Bertrand G. J. Am. Chem. Soc., 2010, 132: 7264-7265
[58] Bates J I, Kennepohl P, Gates D P. Angew. Chem. Int. Ed., 2009, 48: 9844-9847
[59] Mendoza-Espinosa D, Donnadieu B, Bertrand G. Chem.-Asian J., 2011, 6: 1099-1103
[60] Ruiz J, Mesa A F. Chem. Eur. J., 2012, 18: 4485-4488

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