OPTICAL RESOLUTIONS AND CHELATING PROPERTIES OF (PLUS-OR-MINUS)-[2-(METHYLSULFINYL)ETHYL]DIPHENYLARSINE AND ITS PHOSPHORUS ANALOG

被引:88
作者
CHOOI, SYM [1 ]
SIAH, SY [1 ]
LEUNG, PH [1 ]
MOK, KF [1 ]
机构
[1] NATL UNIV SINGAPORE,DEPT CHEM,KENT RIDGE CRESCENT,SINGAPORE 0511,SINGAPORE
关键词
D O I
10.1021/ic00074a026
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
An optical resolution of the asymmetric chelating agents (+/-)-[Ph2ECH2CH2S(O)Me] (E = As or P) has been achieved via fractional crystallization of a pair of diastereomeric palladium(II) complex cations containing the appropriate sulfinyl-substituted ligand and ortho-metalated (S)-(1-(dimethylamino)ethyl)naphthalene. The crystal and molecular structure of the perchlorate salt of the less soluble phosphine-palladium complex has been determined. Crystal data: monoclinic pale yellow prisms, P2(1), a = 10. 147(2) angstrom, h = 10.955(2) angstrom, c = 26.888(5) angstrom, beta = 97.76(2)-degrees, Z = 4, and R = 0.0302. The optically pure compound, [alpha]D-16.1-degrees (c 1.0, dichloromethane), crystallizes as a pair of interconvertible conformers arising from the adoption of different helicities by the nonplanar chelate rings. In both conformers, the sulfinyl-substituted phosphine coordinates to the palladium via phosphorus and oxygen with the uncoordinated sulfur stereocenter of S absolute configuration. Optically pure (S)-[2-(methylsulfinyl)ethyl]-diphenylphosphine, [alpha]D+67.5-degrees (c 1.0, dichloromethane), was displaced from the resolving palladium complex with 1,2-bis(diphenylphosphino)ethane. The (R)-(-)589 enantiomer of the phosphine ligand was obtained in a state of 85% optical purity from the residual mixture of diastereomeric complexes and was subsequently brought to purity by fractional crystallization of the corresponding enantiomorphic complex containing (R)-(1-(dimethylamino)ethyl)naphthalene. Enantiomerically pure forms of [2-(methylsulfinyl)ethyl]diphenylarsine are obtained similarly from the corresponding resolved palladium complexes by treatment with cyanide. The various enantiomeric forms of the sulfinyl-substituted ligands are capable of coordinating to square-planar platinum metal ions via their E, E-0, or E-S donor atoms The mode of coordination is governed by the stereoelectronic factors of the product complexes.
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页码:4812 / 4818
页数:7
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