|
OALib Journal期刊
ISSN: 2333-9721
费用：99美元
|
|
|
|
过渡金属酸盐在催化反应中的应用
, PP. 2287-2298
Keywords: 金属酸盐,金属氧酸盐,卤代金属酸盐,硫代金属酸盐,催化,离子液体
Abstract:
过渡金属酸盐因其催化性能优良、价格低廉、容易获得、毒性低、稳定性良好等特点,成为广受关注的一类催化剂。金属酸盐是指一类含有配合物阴离子的离子型化合物,其配合物阴离子包括中心金属和与其相配位的多个配体基团中心金属为过渡金属元素,配体为氧离子(金属氧酸盐,如WO42-,PMo12O403-等)、硫离子(硫代金属酸盐,如MoS42-等)或卤素离子(卤代金属酸盐,如PtCl62-,TiF62-等)。通过改变中心过渡金属元素和抗衡阳离子的组成,可在分子水平上对金属酸盐进行性能调控。但过渡金属酸盐在催化领域中的研究多集中于金属氧酸盐,本综述则涵盖了包括金属氧酸盐、硫代金属酸盐、氰基金属酸盐和卤代金属酸盐等多种过渡金属酸盐作为催化剂在催化反应中的应用。另外,本文还着重介绍了过渡金属酸盐催化剂与离子液体结合使用,从而实现其循环使用的研究。
| [1] | Gresley N M, Griffith W P, Laemmel A C, Nogueira H I S, Parkin B C. J. Mol. Catal. A: Chem., 1997, 117: 185-198
|
| [2] | Gao J, Chen Y, Han B, Feng Z, Li C, Zhou N, Gao S, Xi Z. J. Mol. Catal. A: Chem., 2004, 210: 197-204
|
| [3] | Weng Z H, Liao G X, Wang J Y, Jian X G. Catal. Commun., 2007, 8: 1493-1496
|
| [4] | Weng Z, Wang J, Jian X. Catal. Commun., 2008, 9: 1688-1691
|
| [5] | Zhang S, Zhao G, Gao S, Xi Z, Xu J. J. Mol. Catal. A: Chem., 2008, 289: 22-27
|
| [6] | Noyori R, Aoki M, Sato K. Chem. Commun., 2003, 1977-1986
|
| [7] | Venturello C, D'Aloisio R. J. Org. Chem., 1988, 53: 1553-1557
|
| [8] | Venturello C, D'Aloisio R, Bart J C J, Ricci M. J. Mol. Catal., 1985, 32: 107-110
|
| [9] | Ishii Y, Yamawaki K, Ura T, Yamada H, Yoshida T, Ogawa M. J. Org. Chem., 1988, 53: 3587-3593
|
| [10] | Matoba Y, Inoue H, Akagi J I, Okabayashi T, Ishii Y, Ogawa M. Synth. Commun., 1984, 14: 865-873
|
| [11] | Grigoropoulou G, Clark J H. Tetrahedron Lett., 2006, 47: 4461-4463
|
| [12] | Hill C L. Chem. Rev., 1998, 98: 1-2
|
| [13] | Hill C L, Prosser-McCartha C M. Coord. Chem. Rev., 1995, 143: 407-455
|
| [14] | Gao F X, Yamase T, Suzuki H. J. Mol. Catal. A: Chem., 2002, 180: 97-108
|
| [15] | Ishikawa E, Yamase T. J. Mol. Catal. A: Chem., 1999, 142: 61-76
|
| [16] | Kholdeeva O A, Maksimov G M, Maksimovskaya R I, Kovaleva L A, Fedotov M A. React. Kinet. Catal. Lett., 1999, 66: 311-317
|
| [17] | Kholdeeva O A, Maksimov G M, Maksimovskaya R I, Kovaleva L A, Fedotov M A, Grigoriev V A, Hill C L. Inorg. Chem., 2000, 39: 3828-3837
|
| [18] | Usui Y, Sato K. Green Chem., 2003, 5: 373-375
|
| [19] | Ren S, Xie Z, Cao L, Xie X, Qin G, Wang J. Catal. Commun., 2009, 10: 464-467
|
| [20] | Vennat M, Herson P, Brégeault J M, Shul'pin G B. Eur. J. Inorg. Chem., 2003, 908-917
|
| [21] | Karimi B, Ghoreishi-Nezhad M, Clark J H. Org. Lett., 2005, 7: 625-628
|
| [22] | Zhu W, Zhu G, Li H, Chao Y, Chang Y, Chen G, Han C. J. Mol. Catal. A: Chem., 2011, 347: 8-14
|
| [23] | Sels B, Vos D D, Buntinx M, Pierard F, Mesmaeker A K, Jacobs P. Nature, 1999, 400: 855-857
|
| [24] | Conte V, Furia F, Moro S. Tetrahedron Lett., 1996, 37: 8609-8612
|
| [25] | Hiskia A, Mylonas A, Papaconstantinou E. Chem. Soc. Rev., 2001, 30: 62-69
|
| [26] | Maldotti A, Molinari A, Amadelli R. Chem. Rev., 2002, 102: 3811-3836
|
| [27] | Mizuno N, Misono M. Chem. Rev., 1998, 98: 199-218
|
| [28] | Molinari A, Varani G, Polo E, Vaccari S, Maldotti A. J. Mol. Catal. A: Chem., 2007, 262: 156-163
|
| [29] | Moriuchi T, Yamaguchi M, Kikushima K, Hirao T. Tetrahedron Lett., 2007, 48: 2667-2670
|
| [30] | Kikushima K, Moriuchi T, Hirao T. Tetrahedron, 2010, 66: 6906-6911
|
| [31] | Yamada T, Sakakura A, Sakaguchi S, Obora Y, Ishii Y. New J. Chem., 2008, 32: 738-742
|
| [32] | Murahashi S, Mitsui H, Shiota T, Tsuda T, Watanabe S. J. Org. Chem., 1990, 55: 1736-1744
|
| [33] | Anandan S, Ryu S Y, Cho W, Yoon M. J. Mol. Catal. A: Chem., 2003, 195: 201-208
|
| [34] | Bai B, Zhao J, Feng X. Mater. Lett., 2003, 57: 3914-3918
|
| [35] | Jiang C J, Guo Y H, Hu C W, Wang C G, Li D F. Mater. Res. Bull., 2004, 39: 251-261
|
| [36] | Yang Y, Wu Q, Guo Y, Hu C, Wang E. J. Mol. Catal. A: Chem., 2005, 225: 203-212
|
| [37] | Li L, Wu Q, Guo Y, Hu C. Micropor. Mesopor. Mater., 2005, 87: 1-9
|
| [38] | Deng Q, Zhou W, Li X, Peng Z, Jiang S, Yue M, Cai T. J. Mol. Catal. A: Chem., 2007, 262: 149-155
|
| [39] | Troupis A, Hiskia A, Papaconstantinou E. Appl. Catal. B: Environ., 2004, 52: 41-48
|
| [40] | Misono M, Nojiri N. Appl. Catal., 1990, 64: 1-30
|
| [41] | Pesaresi L, Brown D R, Lee A F, Montero J M, Williams H, Wilson K. Appl. Catal. A: Gen., 2009, 360: 50-58
|
| [42] | Kozhevnikov I V. Chem. Rev., 1998, 98: 171-198
|
| [43] | Kozhevnikov I V. J. Mol. Catal. A: Chem., 2007, 262: 86-92
|
| [44] | DennyF, Scott J, Chiang K, Teoh W Y, Amal R. J. Mol. Catal. A: Chem., 2007, 263: 93-102
|
| [45] | Hetterley R D, Kozhevnikova E F, Kozhevnikov I V. Chem. Commun., 2006: 782-784
|
| [46] | Welton T. Chem. Rev., 1999, 99: 2071-2084
|
| [47] | Dullius J E L, Suarez P A Z, Einloft S, Souza R F, Dupont J, Fischer J, Cian A D. Organometallics, 1998, 17: 815-819
|
| [48] | Fei Z, Zhao D, Pieraccini D, Ang W H, Geldbach T J, Scopelliti R, Chiappe C, Dyson P J. Organometallics, 2007, 26: 1588-1598
|
| [49] | Bica K, Gaertner P. Org. Lett., 2006, 8: 733-735
|
| [50] | Brown R J C, Dyson P J, Ellis D J, Welton T. Chem. Commun., 2001, 1862-1863
|
| [51] | Cramer S P, Hodgson K O, Gillum W O, Mortenson L E. J. Am. Chem. Soc., 1978, 100: 3398-3407
|
| [52] | Liang K S, Bernholc J, Pan W H, Hughes G J, Stiefel E I. Inorg. Chem., 1987, 26: 1422-1425
|
| [53] | Alonso G, Berhault G, Aguilar A, Collins V, Ornelas C, Fuentes S, Chianelli R R. J. Catal., 2002, 208: 359-369
|
| [54] | Alonso G, Siadati M H, Berhault G, Aguilar A, Fuentes S, Chianelli R R. Appl. Catal. A: Gen., 2004, 263: 109-117
|
| [55] | 牛景扬(Niu J Y), 王敬平(Wang J P). 杂多化合物概论(Introduction of Heteropoly Compound). 开封: 河南大学出版社(Kaifeng: the Press of Henan University), 2000. 365-365
|
| [56] | 孙月霞(Sun Y X), 张志斌(Zhang Z B), 孙琪(Sun Q), 许岩(Xu Y). 无 机 化 学 学 报(Chinese Journal of Inorganic Chemistry), 2011, 27(3): 556-560
|
| [57] | Al-Zahrani S M, Jibril B Y, Abasaeed A E. J. Mol. Catal. A: Chem., 2001, 175: 259-265
|
| [58] | Nowinska K, Sopa M, Waclaw A, Szuba D. Appl. Catal. A: Gen., 2002, 225: 141-151
|
| [59] | Shul'pina L S, Kirillova M V, Pombeiro A J L, Shul'pin G B. Tetrahedron, 2009, 65: 2424-2429
|
| [60] | Chhikara B S, Chandra R, Tandon V. J. Catal., 2005, 230: 436-439
|
| [61] | Kholdeeva O A, Maksimovskaya R I, Maksimov G M, Kovaleva L A. Kinet. Catal., 2001, 42: 217-222
|
| [62] | Kato C N, Negishi S, Yoshida K, Hayashi K, Nomiya K. Appl. Catal. A: Gen., 2005, 292: 97-104
|
| [63] | Sun H, Harms K, Sundermeyer J. J. Am. Chem. Soc., 2004, 126: 9550-9551
|
| [64] | Zhang P, Gong Y, Lv Y, Guo Y, Wang Y, Wang C, Li H. Chem. Commun., 2012, 2334-2336
|
| [65] | Lapisardi G, Chiker F, Launay F, Nogier J P, Bonardet J L. Catal. Commun., 2004, 5: 277-281
|
| [66] | Lee S O, Raja R, Harris K D M, Thomas J M, Johnson B F G, Sankar G. Angew. Chem. Int. Ed., 2003, 42: 1520-1523
|
| [67] | Cheng C Y, Lin K J, Prasad M R, Fu S J, Chang S Y, Shyu S G, Sheu H S, Chen C H, Chuang C H, Lin M T. Catal. Commun., 2007, 8: 1060-1064
|
| [68] | Schmidt A K C, Stark C B W. Org. Lett., 2011, 13: 4164-4167
|
| [69] | Schmidt A K C, Stark C B W. Org. Lett., 2011, 13: 5788-5791
|
| [70] | Sato K, Hyodo M, Aoki M, Zheng X Q, Noyori R. Tetrahedron, 2001, 57: 2469-2476
|
| [71] | Kikushima K, Moriuchi T, Hirao T. Chem. Asian J., 2009, 4: 1213-1216
|
| [72] | Kikushima K, Moriuchi T, Hirao T. Tetrahedron Lett., 2010, 51: 340-342.
|
| [73] | Roy S, Bhar S. Green Chem. Lett. Rev., 2010, 3: 341-347
|
| [74] | Zhu L F, Guo B, Tang D Y, Hu X K, LiG Y, Hu C W. J. Catal., 2007, 245: 446-455
|
| [75] | Murahashi S I, Imada Y, Ohtake H. J. Org. Chem., 1994, 59: 6170-6172
|
| [76] | Arslan-Alaton I, Ferry J L. Dyes Pigments, 2002, 54: 25-36
|
| [77] | Yang Y, Guo Y, Hu C, Wang E. Appl. Catal. A: Gen., 2003, 252: 305-314
|
| [78] | Okumura K, Yamashita K, Hirano M, Niwa M. J. Catal., 2005, 234: 300-307
|
| [79] | Devassy B M, Halligudi S B. J. Catal., 2005, 236: 313-323
|
| [80] | Siddiqui M R H, Holmes S, He H, Smith W, Coker E N, Atkins M P, Kozhevnikov I V. Catal. Lett., 2000, 66: 53-57
|
| [81] | Kozhevnikov I V, Holmes S, Siddiqui M R H. Appl. Catal. A: Gen., 2001, 214: 47-58
|
| [82] | Kozhevnikova E F, Rafiee E, Kozhevnikov I V. Appl. Catal. A: Gen., 2004, 260: 25-34
|
| [83] | Deetlefs M, Raubenheimer H G, Esterhuysen M W. Catal. Today, 2002, 72: 29-41
|
| [84] | Dingwall L D, Corcoran C M, Lee A F, Olivi L, Lynam J M, Wilson K, Catal. Commun., 2008, 10: 53-56
|
| [85] | Bica K, Gaertner P. Eur. J. Org. Chem., 2008, 3453-3456
|
| [86] | Sasaki T, Zhong C, Tada M, Iwasawa Y. Chem. Commun., 2005, 2506-2508
|
| [87] | Sasaki T, Tada M, Zhong C, Kume T, Iwasawa Y. J. Mol. Catal. A: Chem., 2008, 279: 200-209
|
| [88] | Lee C W. Tetrahedron Lett., 1999, 40: 2461-2464
|
| [89] | Abbott A P, Capper G, Davies D L, Rasheed R K, Tambyrajah V. Green Chem., 2002, 4: 24-26
|
| [90] | Dengler J E, Doroodian A, Rieger B. J. Organomet. Chem., 2011, 696: 3831-3835
|
| [91] | Romero-Rivera R, Valle M D, Alonso G, Flores E, Castillón F, Fuentes S, Cruz-Reyes J. Catal. Today, 2008, 130: 354-360
|
Full-Text
|
|
Contact Us
service@oalib.com QQ:3279437679 
WhatsApp +8615387084133
|
|
