RATES OF RING-OPENING OF 2,2,4,7,7-PENTAMETHYL-3,6-DITHIAOCTANE TETRACARBONYL TUNGSTEN (0)
Author:
Affiliation:
1. a Organometallic Chemistry Research Laboratory, Department of Chemistry , University of Puerto Rico , Mayagüez, PR, 00681
Publisher
Informa UK Limited
Subject
Materials Chemistry,Physical and Theoretical Chemistry
Link
https://www.tandfonline.com/doi/pdf/10.1080/00958979808022888
Reference11 articles.
1. Participant of the Undergraduate Research Program of the University of Puerto Rico.
2. Octahedral metal carbonyls. 63. Chelate ring displacement of DTHp from cis-(DTHp)W(CO)4 by Lewis bases (DTHp = 2,2,6,6-tetramethyl-3,5-dithiaheptane, Lewis base = L (phosphine, phosphite))
3. Octahedral metal carbonyls. 66. Rates and mechanism of chelate ring displacement from tetracarbonyltungsten complexes of dithiaalkanes forming seven- and eight-membered chelating rings
4. Solid-state structure and reactivity in solution. 7. Flash photolytic studies of tetracarbonyltungsten(0) intermediates containing five- and six-membered chelating rings coordinating through sulfur
5. Octahedral metal carbonyls
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