同核铁系双金属络合物及其在均相催化体系中的应用

引用本文: 王露, 孙威, 刘超. 同核铁系双金属络合物及其在均相催化体系中的应用[J]. 物理化学学报, 2019, 35(7): 697-708. doi: 10.3866/PKU.WHXB201807071 shu

Citation: WANG Lu, SUN Wei, LIU Chao. Homodinuclear Ferrous Group Metal Complexes and Their Application in Homogeneous Catalysis[J]. Acta Physico-Chimica Sinica, 2019, 35(7): 697-708. doi: 10.3866/PKU.WHXB201807071 shu

同核铁系双金属络合物及其在均相催化体系中的应用

王露 ^1, ,
孙威 ^1,2, ,
刘超 ^{1,
,}

1.
中国科学院兰州化学物理研究所，羰基合成与选择氧化国家重点实验室，兰州 730000
2.
中国科学院大学，北京 100049

作者简介:

刘超，2007年(本科)、2012年(博士)毕业于武汉大学化学与分子科学学院，师从雷爱文教授，随后继续在武汉大学开展博士后研究。博士和博士后期间在英国杜伦大学(2008/10-2009/10)、日本分子科学研究所和名古屋大学(2013/06-08)短期交流学习。自2015年4月起加入中国科学院兰州化物所苏州研究院/羰基合成与选择氧化国家重点实验室开展独立科研工作。入选中国化学会“青年人才托举工程”项目(2016-2018)，荣获“中国催化新秀奖”(2017)。主要从事羰基化学、均相催化研究;

通讯作者: 刘超, chaoliu@licp.cas.cn

基金项目:

国家自然科学基金(91745110, 21673261, 21603245, 21633013, 21703265), 中国科学院兰州化学物理研究所启动基金, 中国科协“青年人才托举工程”项目, 中国科学院青年创新促进会(2018458)以及“西部之光”资助项目

摘要: 随着合成化学的不断发展，开发高活性催化剂来活化一些惰性化学键或者惰性分子受到越来越多的关注。双核金属络合物作为一类特殊的催化剂展现出了不同于单核金属催化剂的催化活性。在双核过渡金属催化体系中，因两个金属中心存在协同作用而表现出了独特的催化活性。铁、钴、镍为第四周期第Ⅷ族元素，也称为铁系元素。该类金属廉价易得且参与的催化反应种类繁多，近年来引起了人们的广泛关注。本综述重点介绍了近年来同核双金属铁系络合物的合成及其表征。同时，对相关同核铁、钴以及镍催化剂在均相催化体系中的应用也进行了详细的介绍和总结。

关键词:

English

Homodinuclear Ferrous Group Metal Complexes and Their Application in Homogeneous Catalysis

WANG Lu ^1, ,
SUN Wei ^1,2, ,
LIU Chao ^{1,
,}

1.
State Key Laboratory for Oxo Synthesis and Selective Oxidation, Lanzhou Institute of Chemical Physics, Chinese Academy of Sciences, Lanzhou 730000, P. R. China
2.
University of Chinese Academy of Sciences, Beijing 100049, P. R. China

Corresponding author: LIU Chao, Email: chaoliu@licp.cas.cn; Tel.: +86-13625299463

Received Date: 28 July 2018
Accepted Date: 04 September 2018
Revised Date: 04 September 2018
Available Online: 15 July 2019
Fund Project:

The project was supported by the National Natural Science Foundation of China (91745110, 21673261, 21603245, 21633013, 21703265), a Start-up Funding from Lanzhou Institute of Chemical Physics (LICP), the Young Elite Scientist Sponsorship Program by Chain Association for Science and Technology (CAST), the Youth Innovation Promotion Association Chinese Academy of Sciences (CAS) (2018458) and the 'Light of West China' Program

Abstract: With the development of synthetic chemistry, more and more efficient catalysts are exploited to activate inert chemical bonds and organic molecules. In the synthetic chemistry, catalysts play an important role, scientists are paying more and more attention to the design and synthesis of catalysts. The majority of catalysts in homogeneous catalytic systems belong to mononuclear active species. In addition to the development of catalysis science, major research is also being conducted on the development of the coordination environment for metal centers to increase their catalytic ability and thereby create enhanced catalytic processes. The catalytic activity of dinuclear catalysts varies from those of mononuclear catalysts. Due to the synergistic effect between the two metal centers, the catalytic activity of dinuclear catalytic systems exhibits particular performance characteristics. The first row of elements in group Ⅷ of the periodic table, Fe, Co, and Ni, are also known as the ferrous group. These metals have drawn attention in recent years because of their relatively low price, stable structure, commercial availability, and ability to catalyze various type of reactions. Homodinuclear ferrous group metal complexes are applied in a wide variety of reactions, including hydroboration, hydrosilylation, cross-coupling reactions, asymmetric 1, 4-addition, asymmetric Mannich reactions, CO₂ activation, copolymerization, and alkyne cyclotrimerizations. Compared with mononuclear metal catalytic systems, there are currently relatively few types of homogenous catalytic systems that are catalyzed by bimetal catalysts. However, such catalytic systems possess significant advantages over mononuclear catalytic systems. For example, the catalytic activity and reaction selectivity of dinuclear metal catalytic systems are far superior, the reaction conditions milder, and the operations required simpler. However, research on the mechanisms of dinuclear metal catalytic systems is still insufficient. For example, the interaction between metals and substrates requires further investigation. This review focusses on the synthesis and characterization of homodinuclear bimetallic iron complexes. The application of homodinuclear iron, cobalt, and nickel complexes in homogeneous catalytic systems is introduced and summarized in detail. Finally, the challenges for the future development of homogeneous catalytic systems that utilize homodinuclear bimetallic iron complexes are outlined.

Key words:

1. [1]
  于卫峰, 孟祥光, 刘莹, 李小红.物理化学学报, 2013, 29, 2041. doi: 10.3866/PKU.WHXB201306282Yu, W. F.; Meng, X. G.; Liu, Y.; Li, X. H. Acta Phys. -Chim. Sin. 2013, 29, 2041. doi: 10.3866/PKU.WHXB201306282
2. [2]
  骆开均, 耿浩, 张晨阳, 倪海亮, 李权.无机化学学报, 2017, 33, 405. doi: 10.11862/cjic.2017.026Luo, K. J.; Geng, H.; Zhang, C. Y.; Ni, H. L.; Li, Q. Chin. J. Inorg. Chem. 2017, 33, 405. doi: 10.11862/cjic.2017.026
3. [3]
  黄斯娉, 袁中直.物理化学学报, 2009, 25, 1599. doi: 10.3866/PKU.WHXB20090753Huang, S. P.; Yuan, Z. Z. Acta Phys. -Chim. Sin. 2009, 25, 1599. doi: 10.3866/PKU.WHXB20090753
4. [4]
  郭莉芹, 史秀丽, 阮文娟, 张晓红, 朱志昂.物理化学学报, 2010, 26, 1195. doi: 10.3866/PKU.WHXB20100336Guo, L. Q.; Shi, X. L.; Ruan, W. J.; Zhang, X. H.; Zhu, Z. A. Acta Phys. -Chim. Sin. 2010, 26, 1195. doi: 10.3866/PKU.WHXB20100336
5. [5]
  刘欢, 臧娜, 赵芳瑶, 刘坤, 李悦, 阮文娟.物理化学学报, 2014, 30, 1801. doi: 10.3866/PKU.WHXB201407171Liu, H.; Zang, N.; Zhao, F. Y.; Liu, K.; Li, Y.; Ruan, W. J. Acta Phys. -Chim. Sin. 2014, 30, 1801. doi: 10.3866/PKU.WHXB201407171
6. [6]
  刘法谦, 赵杰, 张东, 段小群, 王磊, 邓月义, 李伟华.无机化学学报, 2015, 31, 1402. doi: 10.11862/cjic.2015.166Liu, F. Q.; Zhao, J.; Zhang, D.; Duan, X. Q.; Wang, L.; Deng, Y. Y.; Li, W. H. Chin. J. Inorg. Chem. 2015, 31, 1402. doi: 10.11862/cjic.2015.166
7. [7]
  Behlen, M. J.; Zhou, Y. Y.; Steiman, T. J.; Pal, S.; Hartline, D. R.; Zeller, M.; Uyeda, C. Dalton Trans. 2017, 46, 5493. doi: 10.1039/c6dt04465d
8. [8]
  Gavrilova, A. L.; Bosnich, B. Chem. Rev. 2004, 104, 349. doi: 10.1021/cr020604g
9. [9]
  Do, L. H.; Xue, G.; Que, L., Jr.; Lippard, S. J. Inorg. Chem. 2012, 51, 2393. doi: 10.1021/ic202379b
10. [10]
  Ohki, Y.; Hatanaka, T.; Tatsumi, K. J. Am. Chem. Soc. 2008, 130, 17174. doi: 10.1021/ja8063028
11. [11]
  Zhang, F.; Song, H.; Zhuang, X.; Tung, C. H.; Wang, W. J. Am. Chem. Soc. 2017, 139, 17775. doi: 10.1021/jacs.7b11416
12. [12]
  Obligacion, J. V.; Chirik, P. J. Org. Lett. 2013, 15, 2680. doi: 10.1021/ol400990u
13. [13]
  Iovan, D. A.; Betley, T. A. J. Am. Chem. Soc. 2016, 138, 1983. doi: 10.1021/jacs.5b12582
14. [14]
  Tong, P.; Yang, D.; Li, Y.; Wang, B.; Qu, J. Organometallics 2015, 34, 3571. doi: 10.1021/acs.organomet.5b00387
15. [15]
  Wilkinson, E. C.; Dong, Y.; Que, L. J. Am. Chem. Soc. 1994, 116, 8394. doi: 10.1021/ja00097a068
16. [16]
  Mo, Z.; Zhang, Q.; Deng, L. Organometallics 2012, 31, 6518. doi: 10.1021/om300722g
17. [17]
  Chen, Z.; Furutachi, M.; Kato, Y.; Matsunaga, S.; Shibasaki, M. Angew. Chem. Int. Ed. 2009, 48, 2218. doi: 10.1002/anie.200805967
18. [18]
  Gao, J.; Woolley, F. R.; Zingaro, R. A. Org. Biomol. Chem. 2005, 3, 2126. doi: 10.1039/b503971a
19. [19]
  Kember, M. R.; White, A. J. P.; Williams, C. K. Macromolecules 2010, 43, 2291. doi: 10.1021/ma902582m
20. [20]
  Yu, C. Y.; Chuang, H. J.; Ko, B. T. Catal. Sci. Technol. 2016, 6, 1779. doi: 10.1039/c5cy01290b
21. [21]
  Lin, P. -M.; Chang, C. -H.; Chuang, H. -J.; Liu, C. -T.; Ko, B. -T.; Lin, C. -C. ChemCatChem 2016, 8, 984. doi: 10.1002/cctc.201501280
22. [22]
  Chen, Z.; Morimoto, H.; Matsunaga, S.; Shibasaki, M. J. Am. Chem. Soc. 2008, 130, 2170. doi: 10.1021/ja710398q
23. [23]
  Chen, Z.; Yakura, K.; Matsunaga, S.; Shibasaki, M. Org. Lett. 2008, 10, 3239. doi: 10.1021/ol800965t
24. [24]
  Shepherd, N. E.; Tanabe, H.; Xu Y.; Matsunaga, S.; Shibasaki, M. J. Am. Chem. Soc. 2010, 132, 3666. doi: 10.1021/ja1002636
25. [25]
  Mouri, S.; Chen, Z.; Matsunaga, S.; Shibasaki, M. Chem. Commun. 2009, 5138. doi: 10.1039/b912380f
26. [26]
  Shibasaki, M.; Matsunaga, S.; Kato, Y.; Chen, Z. Synlett 2009, 2009, 1635. doi: 10.1055/s-0029-1217192
27. [27]
  Mitsunuma, H.; Matsunaga, S. Chem. Commun. 2011, 47, 469. doi: 10.1039/c0cc02152k
28. [28]
  Xu, Y.; Matsunaga, S.; Shibasaki, M. Org. Lett. 2010, 12, 3246. doi: 10.1021/ol101185p
29. [29]
  Gopinath, P.; Watanabe, T.; Shibasaki, M. Org. Lett. 2012, 14, 1358. doi: 10.1021/ol3002078
30. [30]
  Zhang, S.; Deng, P.; Zhou, J.; Liu, M.; Liang, G.; Xiong, Y.; Zhou, H. Chem. Commun. 2017, 53, 12914. doi: 10.1039/c7cc06468c
31. [31]
  Dible, B. R.; Sigman, M. S. J. Am. Chem. Soc. 2003, 125, 872. doi: 10.1021/ja0286876
32. [32]
  Laskowski, C. A.; Hillhouse, G. L. Organometallics 2009, 28, 6114. doi: 10.1021/om900783u
33. [33]
  Miyazaki, S.; Koga, Y.; Matsumoto, T.; Matsubara, K. Chem. Commun. 2010, 46, 1932. doi: 10.1039/b924716e
34. [34]
  Matsubara, K.; Yamamoto, H.; Miyazaki, S.; Inatomi, T.; Nonaka, K.; Koga, Y.; Yamada, Y.; Veiros, L. F.; Kirchner, K. Organometallics 2016, 36, 255. doi: 10.1021/acs.organomet.6b00451
35. [35]
  Nagao, S.; Matsumoto, T.; Koga, Y.; Matsubara, K. Chem. Lett. 2011, 40, 1036. doi: 10.1246/cl.2011.1036
36. [36]
  Wu, J.; Nova, A.; Balcells, D.; Brudvig, G. W.; Dai, W.; Guard, L. M.; Hazari, N.; Lin, P. H.; Pokhrel, R.; Takase, M. K. Chem. Eur. J. 2014, 20, 5327. doi: 10.1002/chem.201305021
37. [37]
  Durr, A. B.; Fisher, H. C.; Kalvet, I.; Truong, K. N.; Schoenebeck, F. Angew. Chem. Int. Ed. 2017, 56, 13431. doi: 10.1002/anie.201706423
38. [38]
  Yang, X.; Wang, Z. -X. Organometallics 2014, 33, 5863. doi: 10.1021/om500452c
39. [39]
  Zhou, Y. Y.; Hartline, D. R.; Steiman, T. J.; Fanwick, P. E.; Uyeda, C. Inorg. Chem. 2014, 53, 11770. doi: 10.1021/ic5020785
40. [40]
  Steiman, T. J.; Uyeda, C. J. Am. Chem. Soc. 2015, 137, 6104. doi: 10.1021/jacs.5b03092
41. [41]
  Pappas, I.; Treacy, S.; Chirik, P. J. ACS Catal. 2016, 6, 4105. doi: 10.1021/acscatal.6b01134
42. [42]
  Léonard, N. G.; Chirik, P. J. ACS Catal. 2017, 8, 342. doi: 10.1021/acscatal.7b03909
43. [43]
  Pal, S.; Uyeda, C. J. Am. Chem. Soc. 2015, 137, 8042. doi: 10.1021/jacs.5b04990
44. [44]
  Zhou, Y. -Y.; Uyeda, C. Angew. Chem. Int. Ed. 2016, 55, 3171. doi: 10.1002/anie.201511271
45. [45]
  Pal, S.; Zhou, Y. Y.; Uyeda, C. J. Am. Chem. Soc. 2017, 139, 11686. doi: 10.1021/jacs.7b05901
46. [46]
  Hartline, D. R.; Zeller, M.; Uyeda, C. J. Am. Chem. Soc. 2017, 139, 13672. doi: 10.1021/jacs.7b08691
47. [47]
  Rounds, H. R.; Zeller, M.; Uyeda, C. Organometallics 2018, 37, 545. doi: 10.1021/acs.organomet.7b00862
48. [48]
  Powers, I. G.; Andjaba, J. M.; Luo, X.; Mei, J.; Uyeda, C. J. Am. Chem. Soc. 2018, 140, 4110. doi: 10.1021/jacs.8b00503

扫一扫看文章

计量

PDF下载量: 9
文章访问数: 497
HTML全文浏览量: 86

通讯作者: 陈斌, bchen63@163.com

1.
沈阳化工大学材料科学与工程学院沈阳 110142

同核铁系双金属络合物及其在均相催化体系中的应用

通讯作者: 刘超, chaoliu@licp.cas.cn

English

Homodinuclear Ferrous Group Metal Complexes and Their Application in Homogeneous Catalysis

Corresponding author: LIU Chao, Email: chaoliu@licp.cas.cn; Tel.: +86-13625299463

CCS Chemistry：嵌段共聚物自组装成 “三明治”二维有机材料，实现纳米级压力传感功能

CCS Chemistry：颜徐州、鲍哲南：你的皮肤可能是一片SPMs

CCS Chemistry：工作高效不疲劳，只须让催化剂动起来

CCS Chemistry：静电组装导向聚合- 聚电解质纳米凝胶量化制备新策略

CCS Chemistry：金黄色葡萄球菌醛基脱氢酶是如何识别特异性底物的？

计量

通讯作者: 陈斌, bchen63@163.com

中国化学会秘书处

同核铁系双金属络合物及其在均相催化体系中的应用

通讯作者: 刘超, chaoliu@licp.cas.cn

English

Homodinuclear Ferrous Group Metal Complexes and Their Application in Homogeneous Catalysis

Corresponding author: LIU Chao, Email: chaoliu@licp.cas.cn; Tel.: +86-13625299463

CCS Chemistry：嵌段共聚物自组装成 “三明治”二维有机材料，实现纳米级压力传感功能

CCS Chemistry：颜徐州、鲍哲南： 你的皮肤可能是一片SPMs

CCS Chemistry：工作高效不疲劳，只须让催化剂动起来

CCS Chemistry：静电组装导向聚合- 聚电解质纳米凝胶量化制备新策略

CCS Chemistry：金黄色葡萄球菌醛基脱氢酶是如何识别特异性底物的？

计量

文章相关

通讯作者: 陈斌, bchen63@163.com

中国化学会秘书处

CCS Chemistry：颜徐州、鲍哲南：你的皮肤可能是一片SPMs