OBSERVATION OF NEW INTERMEDIATES IN HYDROGENATION CATALYZED BY WILKINSONS CATALYST, RHCL(PPH(3))(3), USING PARAHYDROGEN-INDUCED POLARIZATION

被引:153
作者
DUCKETT, SB
NEWELL, CL
EISENBERG, R
机构
[1] UNIV ROCHESTER, DEPT CHEM, ROCHESTER, NY 14627 USA
[2] UNIV YORK, DEPT CHEM, YORK YO1 5DD, N YORKSHIRE, ENGLAND
关键词
D O I
10.1021/ja00102a023
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Through the use of parahydrogen-induced polarization, the chemistry of RhCl(PPh(3))(3), [RhCl(PPh(3))(2)](2), and RhCl(olefin)(PPh(3))(2) with H-2 and olefinic substrates has been investigated. The phenomenon of PHIP makes possible the detection of previously unobserved dihydride species in the reaction system. Specifically, the binuclear complex H2Rh(PPh3)(2)(mu-Cl)(2)Rh(PPh(3))(olefin) for cis- and trans-2-hexene, 2-pentene, methyl methacrylate, styrene, and substituted styrenes has been detected and characterized. While readily observable during hydrogenation catalysis under ca. 1-2 atm of para-enriched hydrogen, H2Rh(PPh(3))(2)(mu-Cl)(2)Rh(PPh(3))(olefin) is not directly in the catalytic cycle; in fact, its appearance suggests reduced activity of the system through the formation of less active binuclear species. A second new species observed with styrene, p-chlorostyrene, and p-methylstyrene as substrates is the mononuclear complex RhH2(olefin)(PPh(3))(2)(Cl), which appears to be an intermediate in hydrogenation catalysis. From PHIP spectra, it is possible to assign this species as having cis phosphines as well as cis hydrides. The study also underscores the crucial role of PPh(3) at low concentration to inhibit formation of binuclear species in the catalytic system. In a separate experiment, strong polarization for RhH2Cl(PMe(3))(3) is observed, consistent with its poor effectiveness as a catalyst.
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页码:10548 / 10556
页数:9
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共 36 条
[1]   NMR-DETECTION OF INTERMEDIATES DURING HOMOGENEOUS HYDROGENATION OF DIENES USING PARAHYDROGEN [J].
BARGON, J ;
KANDELS, J ;
KATING, P ;
THOMAS, A ;
WOELK, K .
TETRAHEDRON LETTERS, 1990, 31 (40) :5721-5724
[2]   NUCLEAR-MAGNETIC-RESONANCE STUDIES OF HOMOGENEOUS CATALYSIS USING PARAHYDROGEN - ANALYSIS OF NUCLEAR SINGLET TRIPLET MIXING AS A DIAGNOSTIC-TOOL TO CHARACTERIZE INTERMEDIATES [J].
BARGON, J ;
KANDELS, J ;
KATING, P .
JOURNAL OF CHEMICAL PHYSICS, 1993, 98 (08) :6150-6153
[3]   TRANSFORMATION OF SYMMETRIZATION ORDER TO NUCLEAR-SPIN MAGNETIZATION BY CHEMICAL-REACTION AND NUCLEAR-MAGNETIC-RESONANCE [J].
BOWERS, CR ;
WEITEKAMP, DP .
PHYSICAL REVIEW LETTERS, 1986, 57 (21) :2645-2648
[4]   PARA-HYDROGEN AND SYNTHESIS ALLOW DRAMATICALLY ENHANCED NUCLEAR ALIGNMENT [J].
BOWERS, CR ;
WEITEKAMP, DP .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1987, 109 (18) :5541-5542
[5]   SELECTIVITY AND MECHANISM IN CATALYTIC ASYMMETRIC-SYNTHESIS [J].
BROWN, JM .
CHEMICAL SOCIETY REVIEWS, 1993, 22 (01) :25-41
[6]   STRUCTURAL CHARACTERIZATION IN SOLUTION OF INTERMEDIATES IN RHODIUM-CATALYZED HYDROFORMYLATION AND THEIR INTERCONVERSION PATHWAYS [J].
BROWN, JM ;
KENT, AG .
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 2, 1987, (11) :1597-1607
[7]   STEREOCHEMISTRY OF INTERMEDIATES IN HOMOGENEOUS HYDROGENATION CATALYZED BY TRISTRIPHENYLPHOSPHINERHODIUM CHLORIDE, EMPLOYING NUCLEAR-MAGNETIC-RESONANCE MAGNETIZATION TRANSFER [J].
BROWN, JM ;
EVANS, PL ;
LUCY, AR .
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 2, 1987, (11) :1589-1596
[8]   RATES OF CATALYTIC-HYDROGENATION ESTIMATED SPECTROSCOPICALLY THROUGH ENHANCED RESONANCES [J].
CHINN, MS ;
EISENBERG, R .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1992, 114 (05) :1908-1909
[9]   ABINITIO MO STUDY OF THE FULL CATALYTIC CYCLE OF OLEFIN HYDROGENATION BY THE WILKINSON CATALYST RHCL(PR3)3 [J].
DANIEL, C ;
KOGA, N ;
HAN, J ;
FU, XY ;
MOROKUMA, K .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1988, 110 (12) :3773-3787
[10]   MORE THAN INEPT - PARAHYDROGEN AND INEPT+ GIVE UNPRECEDENTED RESONANCE ENHANCEMENT TO C-13 BY DIRECT H-1 POLARIZATION TRANSFER [J].
DUCKETT, SB ;
NEWELL, CL ;
EISENBERG, R .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1993, 115 (03) :1156-1157