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Reaction of Ph2C(X)(CO2H) (X = OH, NH2) with [VO(OR)3] (R = Et, nPr): structure, magnetic susceptibility and ROP capability

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posted on 2024-03-25, 11:46 authored by Mollie A Glenister, Josef Frese, Mark ElsegoodMark Elsegood, Angelos B Canaj, Euan K Brechin, Carl Redshaw

Reaction of [VO(OR)3] (R = Et, nPr) with 2,2’-diphenylglycine afforded the alkoxide-bridged dimers {[VO(OR)(mu-OR)[Ph2C(NH2)(CO2)]}2, whereas use of benzilic acid, in the presence of alkali metals, afforded 16-membered metallocycles {V8(O)4M(OR)8[Ph2C(OH)(CO2)]12} (M = <1 Na, K). For the ring systems, magnetic susceptibility data is consistent with mixed-valance vanadium with an average oxidation state of 3.5. The dimer and ring systems are capable of the ring opening polymerisation (ROP) of ε-caprolactone under N2, air, or as melts affording mostly low to medium molecular weight cyclic and linear products.

Funding

Evolving a circular plastics ecomony

Engineering and Physical Sciences Research Council

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History

School

  • Science

Department

  • Chemistry

Published in

Dalton Transactions

Volume

53

Issue

12

Pages

5351-5355

Publisher

Royal Society of Chemistry (RSC)

Version

  • VoR (Version of Record)

Rights holder

© The Authors

Publisher statement

This is an Open Access Article. It is published by the Royal Society of Chemistry under the Creative Commons Attribution-NonCommercial 3.0 Unported Licence (CC BY-NC). Full details of this licence are available at: https://creativecommons.org/licenses/by-nc/3.0/

Acceptance date

2024-02-26

Publication date

2024-02-27

Copyright date

2024

ISSN

1477-9226

eISSN

1477-9234

Language

  • en

Depositor

Dr Mark Elsegood. Deposit date: 1 March 2024

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