全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用:99美元

查看量下载量

相关文章

更多...
化学进展  2015 

铂配合物类催化剂在γ-氯丙基三氯硅烷合成中的应用

DOI: 10.7536/PC150165, PP. 1182-1190

Keywords: 氯丙基三氯硅烷,硅氢加成,铂配合物,反应机理

Full-Text   Cite this paper   Add to My Lib

Abstract:

γ-氯丙基三氯硅烷是生产硅烷偶联剂的重要中间体,主要通过铂络合物催化氯丙烯和三氯氢硅的硅氢化反应来制备,产业规模早已突破万吨级别。但选择性较低、副产物过多是该产品产业化过程中急需解决的一个关键问题。通过铂催化剂的配体修饰以及催化剂负载的方式,科研工作者在发展高活性高选择性的铂络合物催化剂方面取得了较大成果。本文从均相催化剂以及非均相催化剂两个方面,分别概述了近年来催化该硅氢化反应的铂络合物催化剂和反应机理的研究进展,并对更为高效的铂络合物催化剂的发展进行了展望。

References

[1]  Pietrusza E W, Sommer L H, Whitmore F C. J. Am. Chem. Soc., 1948, 70: 484.
[2]  张先亮(Zhang X L),唐红定(Tang H D),廖俊(Liao J). 硅烷偶联剂-原理、合成与应用(Silane Coupling Agent -Principles, Synthesis and Application). 北京: 化学工业出版社(Beijing: Chemical Industry Press), 2012.
[3]  幸松民(Xing S M), 王一璐(Wang Y L). 有机硅合成工艺及产品应用(The Synthesis and Application of Organic Silicon Products). 北京: 化学工业出版社(Beijing: Chemical Industry Press), 2003.
[4]  Ryan J W, Menzie G K, Speier J L. J. Am. Chem. Soc., 1960, 82: 3601.
[5]  晨光化工研究院编(Edited by Chenguang Chemical Re-search Institute). 有机硅单体及聚合物(The Monomer and Polymer of Organic Silicon). 北京: 化学工业出版社(Beijing: Chemical Industry Press), 1986, 428.
[6]  Белякова З В, Померанцева М Г И, Голубцов С А. ЖОХ. 1964, 35: 1048.
[7]  萧斌(Xiao B). 南昌大学硕士论文(Master Dissertation of Nanchang university), 2006.
[8]  Capka M, Janada M. CS 176909, 1979. CA91: 20704.
[9]  胡春野(Hu C Y), 杨荣华(Yang R H), 江英彦(Jiang Y Y). 分子催化(Journal of Molecular Catalysis). 1988, 2(1): 38.
[10]  沙坚(Sha J), 孙玉滨(Sun Y B), 王毅军(Wang Y J),李力(Li L),王晓方(Wang X F). CN 1056881, 1991.
[11]  Takeuchi M, Endo M, Kubota T, Kiyomori A, Kubota Y. JP 09192494, 1997. CA127: 205701.
[12]  Suzuki M, Imai T. US 4736049, 1998.
[13]  林吉茂(Lin J M), 杨亲正(Yang Q Z), 山东大学学报(自然科学版)(Journal of Shandong University(Natural Science Edition)), 1999, 34(4): 456.
[14]  张中法(Zhang Z F), 黄慧(Huang H),吕彩玲(Lv C L),丁爱梅(Ding A M),郭学阳(Guo X Y),张庆国(Zhang Q G). CN 101624398, 2010.
[15]  丁奎岭(Ding K L),范青华(Fan Q H).不对称催化新概念与新方法(Asymmetric Catalysis: New Concepts and Methods). 北京: 化学工业出版社(Beijing: Chemical Industry Press), 2009.
[16]  Capka M, Janda M. CS 176910, 1979.
[17]  胡春野(Hu C Y), 赵东宇(Zhao D Y), 江英彦(Jiang Y Y). 催化学报(Journal of Catalysis), 1989, 10(2): 213.
[18]  Kiyomori A, Endo M, Kubota T, Kubota Y, Takeuchi M. JP 07325352, 1997.
[19]  Karstedt B. US 3775452 A, 1973.
[20]  汪玉林(Wang Y L), 郑云峰(Zheng Y F), 程建华(Cheng J H),侯建超(Hou J C). 广东化工(Guangdong Chemical Industry). 2010, 37(204): 102.
[21]  Roy A K. Adv. Organomet. Chem., 2008, 55: 1.
[22]  Hopf A, D?tz K H. J. Mol. Catal. A: Chem., 2000, 164: 191.
[23]  MarkóI E, Stérin S, Buisine O, Mignani G, Branlard P, Tinant B, Declercq J-P. Science, 2002, 298: 204.
[24]  Belluco U, Bertani R, Michelin R A, Mozzon M. J. Organomet. Chem., 2000, 600: 37.
[25]  Sprengers J W, Mars M J, Duin M A, Cavell K J, Elsevier C J. J. Organomet. Chem., 2003, 679: 149.
[26]  Isao K, Yohji T, Masuhito O, Tohru K, Kenichi W. US 4292433, 1981.
[27]  Marciniec B, Nowicka T, Mirecki J. PL 156241, 1992.
[28]  Marciniec B, Gulinski J, Mirecki J. PL 162752, 1994.
[29]  Takeuchi M, Endo M, Kubota T, Kiyomori A, Kubota Y. JP 08085624, 1997.
[30]  李月明(Li Y M),范青华(Fan Q H),陈新滋(Chen X Z). 不对称有机反应——催化剂的回收与再利用(Asymmetric Organic Reactions——Recycling and Reuse of Catalysts),北京: 化学工业出版社(Beijing: Chemical Industry Press), 2003.
[31]  Fan Q H, Li Y M, Chan A S C. Chem. Rev., 2002, 102: 3385.
[32]  Wagner G H. US 2637738 A, 1953.
[33]  Thomas K, Steffen S, Christoph B S, Ralf K, Matthias P, Jozef L R H G. US 6153782, 2000.
[34]  Christoph B S, Peter P, Rudolf M, Michael A, Ivo V. US 6472549, 2002.
[35]  Marciniec B, Kornetka Z W, Urbaniak W. J. Mole.Catal., 1981, 12(2): 221.
[36]  何胜刚(He S G). 有机硅材料及应用(Silicone Material and Application). 1991, (4): 16.
[37]  Williams Jr, Robert E. US 4503160, 1985.
[38]  李永军(Li Y J), 江英彦(Jiang Y Y), 催化学报(Journal of Catalysis), 1989, 10(2): 217.
[39]  胡春野(Hu C Y), 汉雪萌(Han X M), 江英彦(Jiang Y Y). 科学通报(Chinese Science Bulletin), 1987, (8): 589.
[40]  Hu C Y, Han X M, Jiang Y Y, Liu J G, Shi T Y. J. Macro-mol. Sci. Chem., 1989, A26(2/3): 349.
[41]  刘继(Liu J),马保德(Ma B D),阳年发(Yang N F),范青华(Fan Q H). 化学进展(Progress in Chemistry), 2010, 22(07): 1457.
[42]  Fan Q H, Deng G J, Feng Y, He Y M. “Enantioselective Catalysis Using Dendrimer Supports” In Handbook of Asym-metric Heterogeneous Catalysis. Ding K, Uozumi Y (Eds). Wiley-VCH: Weinheim, 2008: 131.
[43]  Liu J, Feng Y, Ma B D, He Y M, Fan Q H. Eur. J. Org. Chem. 2012, 34: 6737.
[44]  Drake R A, Griffiths B J, Thomas D R. US 5270424, 1993.
[45]  Dutkiewicz M, Wawrzynczak A, Fiedorow R, Marciniec B, Gulinski J, Maciejewski H A . Pol., 198291, 2008.
[46]  Panster P, Michel R, Buder W, Kleinschmit P. DE 3404703, 1985. CA103: 196232
[47]  Wawrzyńczak A, Dutkiewicz M, Guliński J, Maciejewski H, Marciniec B, Fiedorow R. Catal. Today, 2011, 169: 69.
[48]  Mikami K. 绿色反应介质在有机合成中的应用(Green Reaction Media In Organic Synthesis).王官武(Wang G W), 张泽(Zhang Z),译. 北京: 化学工业出版社(Beijing: Chemical Industry Press), 2007.
[49]  Geisberger G, Auer M, Groessmann A. US 20080045737A1, 2008.
[50]  Geisberger G, Auer M, Groessmann A. CN 101130550, 2008.
[51]  Taccardi N, Fekete M, Berger M E, Stanjek V, Schulz P S, Wasserscheid P. Applied Catalysis A: General, 2011, 399: 69.
[52]  Chalk A J, Harrod J F. J. Am. Chem. Soc., 1965, 87(1): 16.
[53]  Белякова З В, Померанцева М Г И, Белцкова З В. ЖОХ. 1979, 44: 2439.
[54]  Marciniec B, Maciejewski H, Ducamal W, Fiedorow R, Kitynski D. Appl. Organomet. Chem., 2003, 17: 127.
[55]  Gigler P, Drees M, Riener K, Bechlars B, Herrmann W A, Kuhn F E. J. Catal., 2012, 295, 1.
[56]  Sommer L H, Dorfman E, Goldberg G M, Whitmore F C. J. Am. Chem. Soc., 1946, 68: 488.

Full-Text

Contact Us

service@oalib.com

QQ:3279437679

WhatsApp +8615387084133