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Organometallic macrocyclic chemistry. 6.1 Chelate-assisted macrocyclization of 4,7,10-trithiatrideca-2,11-diyne
journal contribution
posted on 2004-01-05, 00:00 authored by A F Hill, A D Rae, Madeleine SchultzMadeleine Schultz, A C WillisThe diyne 4,7,10-trithiatrideca-2,11-diyne (TTDD) reacts smoothly at room temperature with [Ru(CO)2(PPh3)3] to form [Ru(CO)(PPh3) {η4-S(C2H4SCCMe)2CO-κS}], a cyclopentadienone complex in which the unique sulfur atom is also coordinated to the metal but may be displaced by dppe to provide [Ru(CO)(dppe){η4-S(C2H4SCCMe)2CO }]. In contrast, 2,8-decadiyne fails to cyclize even at elevated temperatures, implicating thioether coordination in the mechanism of TTDD macrocyclization.
History
Journal
OrganometallicsVolume
23Issue
1Pagination
81 - 85Publisher
American Chemical SocietyLocation
Washington, D.C.Publisher DOI
ISSN
0276-7333Language
engPublication classification
C Journal article; C1.1 Refereed article in a scholarly journalCopyright notice
2004, American Chemical SocietyUsage metrics
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Categories
Keywords
4,7,10-trithiatrideca-2,11-diyne[Ru(CO)2(PPh3)3]macrocyclic cyclopentadienone complexScience & TechnologyPhysical SciencesChemistry, Inorganic & NuclearChemistry, OrganicChemistryRAY CRYSTAL-STRUCTUREMETAL CLUSTER COMPLEXESSTRUCTURAL CHARACTERIZATIONPOLYTHIAETHER MACROCYCLESCOORDINATIONRUTHENIUMOSMIUMREACTIVITYALKYNESLIGAND