Five-coordinate complexes MHCl(CO)(PiPr3)2 (M = Os, Ru) as precursors for the preparation of new hydrido- and alkenyl-metallothiol and monothio-β-diketonato derivatives

被引:43
作者
Buil, ML [1 ]
Elipe, S [1 ]
Esteruelas, MA [1 ]
Onate, E [1 ]
Peinado, E [1 ]
Ruiz, N [1 ]
机构
[1] Univ Zaragoza, CSIC, Inst Ciencia Mat Aragon, Dept Quim Inorgan, Zaragoza 50009, Spain
关键词
D O I
10.1021/om970633v
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The five-coordinate complexes MHCl(CO)((PPr3)-Pr-i)(2) (M = Os (1), Ru (2)) react with NaSH to give the unsaturated hydrido-metallothiol derivatives MH(SH)(CO)(PiPr3)(2) (M = Os (3), Ru(4)). Complexes 3 and 4 react with CO to afford the cis-dicarbonyl compounds MH(SH)(CO)(2)((PPr3)-Pr-i)(2) (M = Os (5), Ru (6)). Similarly, the reaction of 3 with P(OMe)(3) leads to OsH(SH)(CO){P(OMe)(3)}((PPr3)-Pr-i)(2) (7). Treatment of 3 with 1 equiv of acetylene dicarboxylic methyl ester affords OsH{SC(CO2CH3)CHC(OCH3)O}(CO)((PPr3)-Pr-i)(2) (8), which is the result of the trans addition of the S-H bond of 3 to the carbon-carbon triple bond of the alkyne. The structure of 8 was determined by X-ray investigation. The geometry of the complex can be rationalized as a distorted octahedron with the two phosphorus atoms of the triisopropylphosphine ligands occupying apical positions. The equatorial plane is formed by the bidentate ligand, which acts with a bite angle of 89.49(12)degrees, the hydride ligand trans-disposed to the oxygen atom, and the carbonyl group trans-disposed to the sulfur atom. Acetylenedicarboxylic methyl ester also reacts with 4 by insertion of the carbon-carbon triple bond into the S-H bond. However, in the resulting monothio-beta-diketonato derivative RuH{SC(CO2CH3)CHC(OCH3)O}(CO)((PPr3)-Pr-i)(2) (9) the hydride ligand lies trans to the sulfur atom. In solution, complex 9 isomerizes into 10, containing the hydride ligand trans-disposed to the oxygen atom of the chelate group. The stereochemistry of 10 was corroborated by X-ray investigation. The geometry of 10 is the same as that of 8, and the structural parameters of both molecules are statistically identical. Phenylacetylene and methylpropiolate, in contrast to acetylenedicarboxylic methyl ester, react with 3 and 4 by insertion of the carbon-carbon triple bonds into the M-H bonds to give the unsaturated alkenyl-metallothiol complexes M{(E)CH=CHPh}(SH)(CO)((PPr3)-Pr-i)(2) (M = Os (11), Ru (12)) and Ru{(E)-CH=CHCO2CH3}(SH)(CO)((PPr3)-Pr-i)(2) (13).
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页码:5748 / 5755
页数:8
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共 116 条
[1]   SYNTHESIS AND PROTONATION OF THE DITHIOFORMATO COMPLEX OSH(ETA(2)-S2CH)(CO)(PIPR(3))(2) [J].
ALBENIZ, MJ ;
BUIL, ML ;
ESTERUELAS, MA ;
LOPEZ, AM ;
ORO, LA ;
ZEIER, B .
ORGANOMETALLICS, 1994, 13 (09) :3746-3748
[2]   Synthesis and reactivity of [OsH{C6H4(CH=CHH)}(CO)(PPr3i)(2)] and the formato compounds [Os{(E)-CH=CHPh}(eta(2)-O2CH)(CO)(PPr3i)(2)] and [OsH(eta(2)-O2CH)(CO)(PPr3i)(2)] [J].
Albeniz, MJ ;
Esteruelas, MA ;
Lledos, A ;
Maseras, F ;
Onate, E ;
Oro, LA ;
Sola, E ;
Zeier, B .
JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS, 1997, (02) :181-192
[3]   INTERCONVERSION OF PERSULFIDO, SULFUR HYDRIDE, AND HYDRIDE LIGANDS COORDINATED TO CPRU(PPH3)2+ [J].
AMARASEKERA, J ;
RAUCHFUSS, TB .
INORGANIC CHEMISTRY, 1989, 28 (20) :3875-3883
[4]   KINETIC AND MECHANISTIC INVESTIGATION OF THE SEQUENTIAL HYDROGENATION OF PHENYLACETYLENE CATALYZED BY OSHCL(CO) (PME-TERT-BU2)2, OSHCL(CO)(P-I-PR3)2 [J].
ANDRIOLLO, A ;
ESTERUELAS, MA ;
MEYER, U ;
ORO, LA ;
SANCHEZDELGADO, RA ;
SOLA, E ;
VALERO, C ;
WERNER, H .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1989, 111 (19) :7431-7437
[5]   HETEROGENEOUS CATALYSIS OF THE HYDRODESULFURIZATION OF THIOPHENES IN PETROLEUM - AN ORGANOMETALLIC PERSPECTIVE OF THE MECHANISM [J].
ANGELICI, RJ .
ACCOUNTS OF CHEMICAL RESEARCH, 1988, 21 (11) :387-394
[6]   MONONUCLEAR COMPLEXES OF CR(II) AND FE(II) WITH TERMINAL SH-GROUPS - SYNTHESIS AND X-RAY CRYSTAL-STRUCTURES OF TRANS-M(SH)2(DMPE)2 (M = CR, FE - DMPE = 1,2-BIS(DIMETHYLPHOSPHINO)ETHANE) [J].
ARIF, AM ;
HEFNER, JG ;
JONES, RA ;
KOSCHMIEDER, SU .
JOURNAL OF COORDINATION CHEMISTRY, 1991, 23 (1-4) :13-19
[7]   SYNTHESIS AND STRUCTURAL CHARACTERIZATION OF RUTHENIUM AND OSMIUM CARBONYL CLUSTERS CONTAINING 4,6-DIMETHYLPYRIMIDINE-2-THIONE [J].
AU, YK ;
CHEUNG, KK ;
WONG, WT .
INORGANICA CHIMICA ACTA, 1995, 228 (02) :267-275
[8]   SYNTHESIS, STRUCTURAL CHARACTERIZATION AND THERMAL REACTIVITIES OF OSMIUM CARBONYL CLUSTERS CONTAINING 4,6-DIMETHYLPYRIMIDINE-2-THIONE [J].
AU, YK ;
CHEUNG, KK ;
WONG, WT .
JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS, 1995, (06) :1047-1057
[9]   METALLOCENE SULFIDE CHEMISTRY OF NIOBIUM AND TANTALUM - NEW INSIGHTS INTO THE FORMATION OF NIOBIUM POLYSULFIDO COMPLEXES AND SYNTHESIS, STRUCTURE, AND REACTIVITY OF (CP')2TA(ETA-2-S2)H (CP' = TERT-BUC5H4) [J].
BACH, HJ ;
BRUNNER, H ;
WACHTER, J ;
KUBICKI, MM ;
LEBLANC, JC ;
MOISE, C ;
VOLPATO, F ;
NUBER, B ;
ZIEGLER, ML .
ORGANOMETALLICS, 1992, 11 (03) :1403-1407
[10]   INVESTIGATIONS ON TECHNETIUM AND RHENIUM MONOTHIO-BETA-DIKETONATE COMPLEXES AND X-RAY STRUCTURE OF TRIS(MONOTHIODIBENZOYLMETHANATO)TECHNETIUM(III) [J].
BANDOLI, G ;
MAZZI, U ;
SPIES, H ;
MUNZE, R ;
LUDWIG, E ;
ULHEMANN, E ;
SCHELLER, D .
INORGANICA CHIMICA ACTA, 1987, 132 (02) :177-185