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 

聚乙二醇功能化离子液体的制备及其在有机反应中的应用

DOI: 10.7536/PC150320, PP. 1400-1412

Keywords: 聚乙二醇离子液体,催化,有机合成

Full-Text   Cite this paper   Add to My Lib

Abstract:

聚乙二醇功能化离子液体作为一个新的研究方向受到了化学研究者关注,该类离子液体已经成功地应用于许多有机合成反应中,可以明显改善催化剂性能,并可在一定程度上解决传统催化剂使用中遇到的难分离、难回收再利用的问题。本文介绍了聚乙二醇功能化离子液体的发展历程、制备方法和其作为反应介质、溶剂或催化剂在有机合成反应中应用的最新研究成果,主要包括加成反应、缩合反应、还原反应、酯化反应、硝化反应、氧化反应、水解反应、Heck反应以及Suzuki-Miyaura反应等。

References

[1]  Yang Z Z, Zhao Y N, He L N, Gao J, Yin Z S. Green Chem., 2012, 14(2): 519.
[2]  姚锐(Yao R). 天津大学硕士论文(Master Dissertation of Tianjin University), 2012.
[3]  Smith B M, Graham A E. Tetrahedron Lett., 2006, 47(52): 9317.
[4]  Li D M, Shi F, Peng J J, Guo S, Deng Y Q. J. Org. Chem., 2004, 69(10): 3582.
[5]  职慧珍(Zhi H Z), 罗军(Luo J),马伟(Ma W),吕春绪(Lü C X).高等学校化学学报(Chemical Journal of Chinese University), 2008, 29(10): 2007.
[6]  Zhi H Z, Lu C X, Zhang Q, Luo J. Chem. Commun, 2009, 2878.
[7]  Ablajan K, Maimaiti Z. Synth. Commun., 2012, 42(13): 1959.
[8]  Zou Y, Wu H, Hu Y, Liu H, Zhao X, Ji H L, Shi D Q. Ultrason. Sonochem., 2011, 18(3): 708.
[9]  李晓君(Li X J), 郭红云(Guo H Y). 有机化学(Chinese Journal of Organic Chemistry), 2012, 32(1): 127.
[10]  王英磊(Wang Y L), 罗军(Luo J). 有机化学(Chinese Journal of Organic Chemistry), 2013, 33(9): 2016.
[11]  Luo J, Xin T T, Wang Y L. New J. Chem., 2013, 37(2): 269.
[12]  职慧珍(Zhi H Z), 罗军(Luo J), 马伟(Ma W), 吕春绪(Lv C X). 高等学校化学学报(Chemical Journal of Chinese Universities), 2013, 34(3): 573.
[13]  戴燕(Dai Y), 李斌栋(Li B D), 吕春绪(Lv C X). 精细石油化工(Speciality Petrochemicals), 2009, 26(2): 40.
[14]  Tan B, Jiang J Y, Wang Y H, Wei L, Chen D J, Jin Z L. Appl. Organomet. Chem., 2008, 22(11): 620.
[15]  Zeng Y, Wang Y H, Jiang J Y, Jin Z L. Catal. Commun., 2012, 19: 70.
[16]  Wei L, Jiang J Y, Wang Y H, Jin Z L. J. Mol. Catal. A: Chem., 2004, 221(1/2): 47.
[17]  郑明东(Zheng M D), 陈同云(Chen T Y ), 胡克良(Hu K L).高等学校化学学报(Chemical Journal of Chinese Universities), 2006, 27(6): 1086.
[18]  王会萍(Wang H P), 商艳梅(Shang Y M), 王磊(Wang L), 李叶芝(Li Y Z), 黄化民(Huang H M). 高等学校化学学报(Chemical Journal of Chinese Universities), 2006, 27(5): 894.
[19]  职慧珍(Zhi H Z), 罗军(Luo J), 马伟(Ma W), 吕春绪(Lv C X). 高等学校化学学报(Chemical Journal of Chinese Universities), 2008, 29(4): 772.
[20]  Wu Q, Wan H, Li H, Song H, Chu T. Catal. Today, 2013, 200(1): 74.
[21]  Laali K K, Gettwert V J. J. Org. Chem., 2001, 66(1): 35.
[22]  Smith K, Liu S, El-Hiti G A. Ind. Eng. Chem. Res., 2005, 44(23): 8611.
[23]  Fang D, Shi Q R, Cheng J, Gong K, Liu Z L. Appl. Catal. A, 2008, 345(2): 158.
[24]  Lee S G. Chem. Commun., 2006, 10: 1049.
[25]  Pucheault M, Vaultier M. Top Curr. Chem., 2009, 290: 83.
[26]  Giernoth R. Angew Chem. Int. Ed., 2010, 49(16): 2834.
[27]  应安国(Ying A G), 叶伟东(Ye W D), 刘泺(Liu L), 吴国锋(Wu G F), 陈新志(Chen X Z), 钱胜(Qian S), 张秋萍(Zhang Q P). 有机化学(Chinese Journal of Organic Chemistry), 2008, 28(12): 2081.
[28]  钟涛(Zhong T), 乐长高(Le Z G), 谢宗波(Xie Z B), 曹霞(Cao X), 吕雪霞(Lv X X). 有机化学(Chinese Journal of Organic Chemistry), 2010, 30(7): 981.
[29]  Chen J, Spear S K, Huddleston J G, Holbrey J D, Swatloski R P, Rogers R D. Green Chem., 2004, 43(17): 5358.
[30]  Naik S D, Doraiswamy L K. AIChE J., 1998, 44(3): 612.
[31]  Chen J, Spear S K, Huddleston J G, Rogers R D. Green Chem., 2005, 7(2): 64.
[32]  Chandrasekhar S, Prakash S J, Rao C L. J. Org. Chem., 2006, 71(5): 2196.
[33]  Fraga D J, Famelart M H, Bazureau J P. Org. Proc. Res. Dev., 2002, 6(4): 374.
[34]  Jin C M, Ye C F, Phillips B S, Zabinski J S, Liu X Q, Liu W M, Shreeve J M. J. Mater. Chem., 2006, 16(16): 1529.
[35]  Zhi H Z, Lv C X, Zhang Q, Luo J. Chem. Commun., 2009, 20: 2878.
[36]  Li H, Hou Z S, Qiao Y X, Feng B, Hu Y, Wang X R, Zhao X G. Catal. Commun., 2010, 11(5): 470.
[37]  Williams M E, Masui H, Long J W, Malik J, Murray R W. J. Am. Chem. Soc., 1997, 119(8): 1997.
[38]  Masui H, Murray R W. Inorg. Chem., 1997, 36(22): 5118.
[39]  Long J W, Kim I K, Murray R W. J. Am.Chem. Soc., 1997, 119(47): 11510.
[40]  Williams M E, Crooker J C, Pyati R, Lyons L J, Murray R W. J. Am. Chem. Soc., 1997, 119(42): 10249.
[41]  Dickinson V E, Williams M E, Hendrichson S M, Masui H, Murray R W. J. Am. Chem. Soc., 1999, 121(4): 613.
[42]  Liu N, Liu C, Jin Z.Green Chem., 2012, 14(3): 592.
[43]  付尧(Fu Y). 大连理工大学硕士学位论文(Master Dissertation of Dalian University of Technology), 2014.
[44]  姚美焕(Yao M H), 梁永民(Liang Y M), 夏延秋(Xia Y F), 周峰(Zhou F). 2009年全国摩擦学学术会议(The 2009 National Conference on Tribology),长沙(Changsha). 379.
[45]  Wu C, Peng J J, Li J Y, Bai Y, Hu Y Q, Lai G Q. Catal. Commun., 2008, 10(2): 248.
[46]  Xu Y S, Bai Y, Peng J J, Li J Y, Xiao W J, Lai G Q. J. Organomet. Chem., 2014, 765: 59.
[47]  Calo V, Nacci A, Monopoli A, Fanizzi A. Org. Lett., 2002, 4(15): 2561.
[48]  Nishikubo T, Kameyama A, Yamashita J, Tomoi M, Fukuda W. J. Polym. Sci. Part A: Polym. Chem., 1993, 31(4): 939.
[49]  Nishikubo T, Kameyama A, Yamashita J, Fukumitsu T, Maejima C, Tomoi M. J. Polym. Sci. Part A: Polym. Chem., 1995, 33(7): 1011.
[50]  Ochiai B, Endo T. J. Polym. Sci. Part A: Polym. Chem., 2007, 45(23): 5673.
[51]  Takeda N, Inoue S. Bull. Chem. Soc. Jpn., 1978, 51(12): 3564.
[52]  Kasuga K, Kato T, Kabata N, Handa M. Bull. Chem. Soc. Jpn., 1996, 69(10): 2885.
[53]  Jin L L, Jing H W, Chang T, Bu X L, Wang L, Liu Z L. J. Mol. Catal. A: Chem., 2007, 261(2): 262.
[54]  Fujinami T, Suzuki T, Kamiya M, Fukuzawa S, Sakai S. Chem. Lett., 1985, 14(2): 199.
[55]  Melendez J, North M, Pasquale R. Eur. J. Inorg. Chem., 2007, 21: 3323.
[56]  North M, Pasquale R. Angew. Chem. Int. Ed., 2009, 48(16): 2946.
[57]  Berkessel A, Brandenburg M. Org. Lett., 2006, 8(20): 4401.
[58]  职慧珍(Zhi H Z). 南京理工大学博士论文(Doctoral Dissertation of Nanjing University of Science and Technology), 2012.
[59]  Wang Y L, Li Z, Luo J, Liu Z L. J. Chin. Chem. Soc., 2013, 60(12): 1431.
[60]  Kuo S C, Huang L J, Nakamura H. Med. Chem., 1984, 27(4): 539.
[61]  史达清(Shi D Q), 张姝(Zhang S), 庄启亚(Zhuang Q Y), 屠树江(Tu S J), 胡宏纹(Hu H W). 有机化学(Chinese Journal of Organic Chemistry), 2003, 23(11): 1314.
[62]  Mecadon H, Rohman M R, Kharbangar I, Laloo B M, Kharkongor I, Rajbangshi M, Myrboh B. Tetrahedron Lett., 2011, 52(25): 3228.
[63]  Litvinov Y M, Shestopalov A A, Rodinovskaya L A, Shestopalov A M. J. Comb. Chem., 2009, 11(5): 914.
[64]  Wang P C, Lu M. Tetrahedron Lett., 2011, 52(13): 1452.
[65]  Mallat T, Baiker A. Chem. Rev., 2004, 104(6): 3037.
[66]  Ghorbani-Choghamarani A, Azadi G. J. Iran. Chem. Soc., 2011, 8(4): 1082.
[67]  Hajipour A R, Khazdooz L, Ruoho A E. J. Iran. Chem. Soc., 2011, 8(2): 382.
[68]  Hu Y L, Lu M, Ge X T. J. Iran. Chem. Soc., 2013, 10(3): 453.
[69]  Lu T T, Mao Y, Yao K, Xu J, Lu M. Catal. Commun., 2012, 27: 124.
[70]  Beste G W, Hammett L P. J. Am. Chem. Soc., 1940, 62: 2481.
[71]  Saramma K, Anantarman R. Proc. Indian Acad. Sci. Sect. A, 1959, 49(2): 111.
[72]  Shi M, Feng Y S. J. Org. Chem., 2001, 66(9): 3235.
[73]  Leonid G M, Andrei V V, Olga S K, Oleg M N. Mendeleev Commun., 1995, 5(6): 223.
[74]  Xing M K, Si Q C, Juan D, Xiao Q Y, Xian C Z. J. Mol. Catal. A: Chem., 2004, 210(1/2): 23.
[75]  Bazzicalupi C, Bencini A, Berni E, Di Vaira M. Inorg. Chim. Acta, 2005, 358: 77.
[76]  Mohile S S, Potdar M K, Harjani J R, Nara S J, Salunkhe M M, Swapnil S M, Mahesh K P. J. Mol. Catal. B: Enzylmatic., 2004, 30(5/6): 185.
[77]  蒋辉(Jiang H), 陆明(Lu M). 南京理工大学硕士论文, (Master Dissertation of Nanjing University of Science and Technology), 2011.
[78]  Hu Y L, Jiang H, Zhu J, Lu M. New J. Chem., 2011, 35(2): 292.
[79]  Wang L, Zhang Y H, Xie C S, Wang Y G. Synlett, 2005, 12: 1861.
[80]  Li B, Li Y Q, Zheng J. ARKIVOC, 2010, 9: 163.
[81]  Wang J Y, Xu B L, Sun H Y, Song G H. Tetrahedron Lett., 2013, 54(3): 238.
[82]  Wang Y L, Luo J, Liu Z L. Appl. Organomet. Chem., 2013, 27(10): 601.
[83]  Hu Y L, Lu M, Ge Q, Wang P C, Lu T T. J. Ind. Eng. Chem., 2010, 16 (4): 615.
[84]  陆鸿飞(Lu H F), 孙垒垒(Sun L L), 武鼎铭(Wu D M),高玉华(Gao Y H), 石亚丽(Shi Y L), 薛芹(Xue Q). 有机化学(Chinese Journal of Organic Chemistry), 2012, 32(10): 1880.

Full-Text

Contact Us

service@oalib.com

QQ:3279437679

WhatsApp +8615387084133