Optically Active Transition Metal Compounds, 136 [1]. An Octahedral Molybdenum Complex (P-P’)Mo(CO)4 with a Chiral Secondary Phosphorus Atom

2004 ◽  
Vol 59 (8) ◽  
pp. 889-892
Author(s):  
Henri Brunner ◽  
Ilias Grau ◽  
Manfred Zabel

AbstractReaction of (η6-C6H5CH3)Mo(CO)3 with the easily accessible chiral chelate ligand P,P,Pʹ-tris- [(+)-9-phenyldeltacyclan-8-yl]-1,2-bis(phosphanyl)benzene P-P’ afforded the octahedral molybdenum carbonyl derivate (P-P’)Mo(CO)4 1 as a diastereomer mixture 1a (74%) and 1b (26%). Crystallization gave single crystals of (SP)-(P-P’)Mo(CO)4 1a. The X-ray structure analysis of compound 1a revealed the formation of an unusual triple-decker π-stack in the solid state.

1998 ◽  
Vol 558 (1-2) ◽  
pp. 213-218 ◽  
Author(s):  
Henri Brunner ◽  
Andreas Winter ◽  
Bernhard Nuber

1991 ◽  
Vol 46 (8) ◽  
pp. 1025-1030 ◽  
Author(s):  
Kurt Merzweiler ◽  
Hans-Jörg Kersten

The reaction of [{(CO)5Cr}(Ph2PCl)] with (Me3Si)2Se in toluene at 298 K leads to the compounds [{(CO)5Ph2P}2Se] (1) and [{(CO)5Cr}(Ph2P)2Se] (2). If the reaction is carried out in ether as solvent at 308 K, [{(CO)4Cr}(Ph2P)2Se] (3) is obtained. The structures of 1, 2 and 3 were determined by single crystal X-ray analysis. 1, 2 and 3 contain the Ph2PSePPh2 ligand, which is coordinated to chromium carbonyl fragments in three different ways. 1 consists of a dinuclear complex in which two {(CO)5Cr} fragments are linked by a Ph2PSePPh2 group. In 2, only one phosphorus atom of the Ph2PSePPh2 ligand is bound to a {(CO)5Cr} unit. In 3, the Ph2PSePPh2 group is coordinated as a chelate ligand to a {(CO)4Cr} fragment.


1998 ◽  
Vol 556 (1-2) ◽  
pp. 129-140 ◽  
Author(s):  
Henri Brunner ◽  
Peter Faustmann ◽  
Bernhard Nuber

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