Effect of the leaving ligand X on transmetalation of organostannanes (vinylSnR3) with LnPd(Ar)(X) in Stille cross-coupling reactions.: A density functional theory study

被引:56
作者
Ariafard, Alireza
Lin, Zhenyang
Fairlamb, Ian J. S.
机构
[1] Islamic Azad Univ, Dept Chem, Fac Sci, Cent Tehran Branch, Tehran, Iran
[2] Hong Kong Univ Sci & Technol, Dept Chem, Kowloon, Hong Kong, Peoples R China
[3] Univ York, Dept Chem, York YO10 5DD, N Yorkshire, England
关键词
D O I
10.1021/om0607705
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Density functional theory calculations were carried out to study the effect of different leaving ligands X on transmetalation of organostannanes (vinylSnR(3)) with LnPd(Ar)(X) (X = Cl, Br, I), an important step found in Stille cross-coupling processes. The calculations indicate that the overall activation barriers for the transmetalation process increase in the following order: X = Cl < Br < I. The model phosphine ligands, PH3 and PMe3, were used to investigate this process. It was established that more electron-donating phosphine ligands significantly increase the overall transmetalation barriers.
引用
收藏
页码:5788 / 5794
页数:7
相关论文
共 66 条
[1]   Computational characterization of a complete palladium-catalyzed cross-coupling process:: The associative transmetalation in the Stille reaction [J].
Alvarez, R ;
Faza, ON ;
López, CS ;
de Lera, AR .
ORGANIC LETTERS, 2006, 8 (01) :35-38
[2]   Understanding the relative easiness of oxidative addition of aryl and alkyl halides to palladium(0) [J].
Ariafard, Alireza ;
Lin, Zhenyang .
ORGANOMETALLICS, 2006, 25 (16) :4030-4033
[3]   DENSITY-FUNCTIONAL THERMOCHEMISTRY .3. THE ROLE OF EXACT EXCHANGE [J].
BECKE, AD .
JOURNAL OF CHEMICAL PHYSICS, 1993, 98 (07) :5648-5652
[4]   A new precatalyst for the Suzuki reaction -: a pyridyl-bridged dinuclear palladium complex as a source of mono-ligated palladium(0) [J].
Beeby, A ;
Bettington, S ;
Fairlamb, IJS ;
Goeta, AE ;
Kapdi, AR ;
Niemelä, EH ;
Thompson, AL .
NEW JOURNAL OF CHEMISTRY, 2004, 28 (05) :600-605
[5]   The heck reaction as a sharpening stone of palladium catalysis [J].
Beletskaya, IP ;
Cheprakov, AV .
CHEMICAL REVIEWS, 2000, 100 (08) :3009-3066
[6]   Computational characterization of the role of the base in the Suzuki-Miyaura cross-coupling reaction [J].
Braga, AAC ;
Morgon, NH ;
Ujaque, G ;
Maseras, F .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2005, 127 (25) :9298-9307
[7]   Advances in functional-group-tolerant metal-catalyzed alkyl-alkyl cross-coupling reactions [J].
Cárdenas, DJ .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2003, 42 (04) :384-387
[8]   OXIDATIVE ADDITION OF CATIONIC (ETA(6)-CHLOROARENE)TRICARBONYLMANGANESE COMPOUNDS TO PALLADIUM(O) COMPLEXES - SYNTHESIS, CHARACTERIZATION AND REACTIVITY [J].
CARPENTIER, JF ;
CASTANET, Y ;
BROCARD, J ;
MORTREUX, A ;
ROSEMUNCH, F ;
SUSANNE, C ;
ROSE, E .
JOURNAL OF ORGANOMETALLIC CHEMISTRY, 1995, 493 (1-2) :C22-C24
[9]   On the configuration resulting from oxidative addition of RX to Pd(PPh3)4 and the mechanism of the cis-to-trans isomerization of [PdRX(PPh3)2] complexes (R equals aryl, X equals halide) [J].
Casado, AL ;
Espinet, P .
ORGANOMETALLICS, 1998, 17 (05) :954-959
[10]   Mechanism of the Stille reaction.: 1.: The transmetalation step.: Coupling of R1I and R2SnBu3 catalyzed by trans-[PdR1IL2] (R1 = C6Cl2F3; R2 = vinyl, 4-methoxyphenyl; L = AsPh3) [J].
Casado, AL ;
Espinet, P .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1998, 120 (35) :8978-8985