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   <subfield code="a">Synthesis, Characterization and Catalytic Activity Studies of Rhenium Carbonyl Complexes Containing Chiral Diphosphines of the Josiphos and Walphos Families</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Ahmed Abdel-Magied, Manjula Patil, Amrendra Singh, Matti Haukka, Magda Monari, Ebbe Nordlander]</subfield>
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   <subfield code="a">Ten rhenium carbonyl complexes—[Re(H)(CO)3(1a)], [Re3(µ-H)3(CO)10(1a)], [Re2(CO)9(2a)], [Re2(CO)8(2a)], [Re2(CO)9(2b)], [{Re2(CO)9}2(2b)], [Re2(CO)8(2b)], [Re2(CO)8(1b)], [Re2(µ-H)2(CO)6(2b)] and [Re3(µ-H)3(CO)11(2b)]—containing different bidentate chiral phosphine ligands of the Josiphos (1a, 1b) and Walphos (2a, 2b) families have been synthesized and fully characterized (1a: (R)-1-{(S P)-2-[Bis[3,5-bis(trifluoromethyl)phenyl]phosphino]ferrocenyl}ethyldi(3,5-xylyl)phosphine, 1b: (R)-1-{(S P)-2-[Di(2-furyl)phosphino]ferrocenyl}ethyldi-tert-butylphosphine, 2a: (R)-1-{(R P)-2-[2-[Bis(4-methoxy-3,5-dimethylphenyl)phosphino]phenyl]ferrocenyl}ethylbis[3,5-bis(trifluoromethyl)phenyl]phosphine and 2b: (R)-1-{(R P)-2-[2-(Diphenylphosphino)phenyl]ferrocenyl}ethyldicyclohexylphosphine). The phosphine-substituted clusters were tested for hydrogenation of tiglic acid [trans-2-methyl-2-butenoic acid]. The catalytic reactions gave reasonable conversion rates (15-88%) under relatively mild conditions but relatively moderate enantiomeric excesses (8-57%) were observed. The crystal structures of [ReH(CO)3(1a)], [Re2(CO)9(2a)], [{Re2(CO)9}2(2b)] and [Re2(µ-H)2(CO)6(2b)] are presented.</subfield>
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   <subfield code="a">Singh</subfield>
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   <subfield code="u">Inorganic Chemistry Research Group, Chemical Physics, Center for Chemistry and Chemical Engineering, Lund University, Box 124, 221 00, Lund, Sweden</subfield>
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   <subfield code="a">Haukka</subfield>
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   <subfield code="u">Department of Chemistry, University of Jyväskylä, Box 35, 40014, Jyväskylä, Finland</subfield>
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   <subfield code="a">Metadata rights reserved</subfield>
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