Organometallic Macrocyclic Chemistry. 6.1 Chelate-Assisted Macrocyclization of 4,7,10-Trithiatrideca-2,11-diyne

Hill, Anthony F., Rae, A. David, Schultz, Madeleine, & Willis, Anthony C. (2004) Organometallic Macrocyclic Chemistry. 6.1 Chelate-Assisted Macrocyclization of 4,7,10-Trithiatrideca-2,11-diyne. Organometallics, 23(1), pp. 81-85.

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The 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){4-S(C2H4SCCMe)2CO-S}], 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){4-S(C2H4SCCMe)2CO}]. In contrast, 2,8-decadiyne fails to cyclize even at elevated temperatures, implicating thioether coordination in the mechanism of TTDD macrocyclization.

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ID Code: 8743
Item Type: Journal Article
Refereed: Yes
Additional Information: This article is freely available from the American Chemical Society website 12 months after the publication date. See links to publisher website in this record.
DOI: 10.1021/om0305723
Subjects: Australian and New Zealand Standard Research Classification > CHEMICAL SCIENCE (030000) > OTHER CHEMICAL SCIENCES (039900) > Organometallic Chemistry (039904)
Divisions: Past > QUT Faculties & Divisions > Faculty of Science and Technology
Copyright Owner: Copyright 2004 American Chemical Society
Deposited On: 17 Aug 2007 00:00
Last Modified: 29 Feb 2012 13:41

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