Synthesis and ROMP Chemistry of Decafluoroterphenoxide Molybdenum Imido Alkylidene and Ethylene Complexes

被引:29
作者
Yuan, Jian [1 ]
Schrock, Richard R. [1 ]
Gerber, Laura C. H. [1 ]
Mueller, Peter [1 ]
Smith, Stacey [1 ]
机构
[1] MIT, Dept Chem 6 331, Cambridge, MA 02139 USA
基金
美国国家科学基金会;
关键词
OPENING METATHESIS POLYMERIZATION; MO; PYRROLIDE; EFFICIENT; PRECURSORS; CATALYSTS; METAL;
D O I
10.1021/om400199u
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The bisDFTO alkylidene complexes of molybdenum Mo(NR)(CHCMe2Ph)(DFTO)(2) (R = 2,6-i-Pr2C6H3, 2,6-Me2C6H3, C6F5, 1-adamantyl; DFTO = 2,6-(C6F5)(2)C6H3O) and monoarylcodde monopyrrolide (MAP) complexes Mo(NR)(CHCMe2Ph)(Me(2)Pyr)-(OAr) (Me(2)Pyr = 2,S-dimethylpyrrolide; R = C6F3, OAr = DFTO, 2,6dimesitylphenoxide (HMTO); R = 2,6-Me2C6H3, OAr = DFTO) have been prepared in good yields. Addition of dicarbomethoxynorbornadiene (DCMNBD) to bisDFTO complexes yielded polymers that have a cis,isotactic structure. Polymerization of DCMNBD by Mo(NC6F5)-(CHCMeiPh)(Me(2)Pyr)(HMTO) gives a polymer that contains the expected cis,syndiotactic structure, but polymerization of DCMNBD by Mo(NR)(CHCMe2Ph)(Me(2)Pyr)(DFTO) (R = C6F5, 2,6-Me2C6H3) generates a polymer that has a cis,isotactic structure, the first observation of a cis,isotactic polymer prepared employing a MAP initiator. Norbornene is polymerized to give what is proposed to be highly tactic cis-polyNBE. Addition of ethylene to Mo(NC6F5)(CHCMe2Ph)(DFTO)(2) leads to formation of Mo(NC6F5)(CH2CH2)-(DFTO)(2), which also behaves as an initiator for polymerization of DCMNBD to cis,isotactic-polyDCMNBD and norbornene to cis highly tactic polyNBE. Mo(NC6F5)(CH2CH2)(DFT0)2 reacts with 3-methyl-3-phenylc-yclopropene (MPCP) to give Mo(NC6F5)(CHCHCMePh)(DFTO)(2) in similar to 50% yield.
引用
收藏
页码:2983 / 2992
页数:10
相关论文
共 38 条
[11]   Olefin-metathesis catalysts for the preparation of molecules and materials (Nobel lecture) [J].
Grubbs, Robert H. .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2006, 45 (23) :3760-3765
[12]   Thermodynamics, kinetics, and mechanism of (silox)3M(olefin) to (silox)3M(alkylidene) rearrangements (silox = tBu3SiO; M = Nb, Ta) [J].
Hirsekorn, KF ;
Veige, AS ;
Marshak, MP ;
Koldobskaya, Y ;
Wolczanski, PT ;
Cundari, TR ;
Lobkovsky, EB .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2005, 127 (13) :4809-4830
[13]   Highly Z- and Enantioselective Ring-Opening/Cross-Metathesis Reactions Catalyzed by Stereogenic-at-Mo Adamantylimido Complexes [J].
Ibrahem, Ismail ;
Yu, Miao ;
Schrock, Richard R. ;
Hoveyda, Amir H. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2009, 131 (11) :3844-+
[14]  
IVIN KJ, 1977, MAKROMOL CHEM, V178, P1545
[15]   Cationic molybdenum imido alkylidene complexes [J].
Jiang, Annie J. ;
Schrock, Richard R. ;
Mueller, Peter .
ORGANOMETALLICS, 2008, 27 (17) :4428-4438
[16]   Highly Z-Selective Metathesis Homocoupling of Terminal Olefins [J].
Jiang, Annie J. ;
Zhao, Yu ;
Schrock, Richard R. ;
Hoveyda, Amir H. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2009, 131 (46) :16630-+
[17]   Fundamental Studies of Tungsten Alkylidene Imido Monoalkoxidepyrrolide Complexes [J].
Jiang, Annie J. ;
Simpson, Jeffrey H. ;
Mueller, Peter ;
Schrock, Richard R. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2009, 131 (22) :7770-7780
[18]   SYNTHESIS OF TUNGSTEN VINYL ALKYLIDENE COMPLEXES VIA THE REACTIONS OF WCL2(NAR)(PX3)3 (X = R, OME) PRECURSORS WITH 3,3-DISUBSTITUTED CYCLOPROPENES [J].
JOHNSON, LK ;
GRUBBS, RH ;
ZILLER, JW .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1993, 115 (18) :8130-8145
[19]   Syntheses of Variations of Stereogenic-at-Metal Imido Alkylidene Complexes of Molybdenum [J].
Marinescu, Smaranda C. ;
Ng, Victor W. L. ;
Lichtscheidl, Alejandro G. ;
Schrock, Richard R. ;
Mueller, Peter ;
Takase, Michael K. .
ORGANOMETALLICS, 2012, 31 (17) :6336-6343
[20]   Room-Temperature Z-Selective Homocoupling of α-Olefins by Tungsten Catalysts [J].
Marinescu, Smaranda C. ;
Schrock, Richard R. ;
Mueller, Peter ;
Takase, Michael K. ;
Hoveyda, Amir H. .
ORGANOMETALLICS, 2011, 30 (07) :1780-1782