Petrov, Andrey, Conrad, Lawrence, Coles, Nathan T. ![]() ![]() |
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Official URL: https://doi.org/10.1002/chem.202203056
Abstract
A diglyme solution of Na[cyclo-P5] (1) reacts with alkynes and isolobal nitriles and phosphaalkynes to afford the otherwise elusive (aza)phospholide anions 2 a–c, 4 a,b, and 6. The reaction of Na[cyclo-P5] with alkynes and nitriles was studied by means of DFT methods, which suggested a concerted mechanism for the formation of 2 a and 4 b. The anions 2 a–c, 4 a,b, and 6 coordinate in an η5-fashion towards FeII to give the sandwich (aza)phosphametallocenes 3 a–c, 5 a,b and 7 in moderate to good yields. The new compounds were characterized by means of multinuclear NMR spectroscopy, single-crystal X-ray diffraction and cyclic voltammetry.
Item Type: | Article |
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Date Type: | Publication |
Status: | Published |
Schools: | Chemistry |
Publisher: | Wiley |
ISSN: | 0947-6539 |
Date of First Compliant Deposit: | 4 December 2024 |
Date of Acceptance: | 9 October 2022 |
Last Modified: | 06 Jan 2025 10:07 |
URI: | https://orca.cardiff.ac.uk/id/eprint/173588 |
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