Loading…
Solvent Dependence of the Structure of Ethylzinc Acetate and Its Application in CO2/Epoxide Copolymerization
NMR and single-crystal X-ray diffraction experiments indicate that the ligand stoichiometry of the complexes formed from the reaction between zinc bis(acetate) and diethylzinc depends on the nature of the solvent (coordinating vs noncoordinating) and that the strength of the donor interaction of a c...
Saved in:
Published in: | Organometallics 2011-04, Vol.30 (8), p.2223-2229 |
---|---|
Main Authors: | , , , , |
Format: | Article |
Language: | English |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | |
---|---|
cites | |
container_end_page | 2229 |
container_issue | 8 |
container_start_page | 2223 |
container_title | Organometallics |
container_volume | 30 |
creator | Orchard, Katherine L Harris, Jonathan E White, Andrew J. P Shaffer, Milo S. P Williams, Charlotte K |
description | NMR and single-crystal X-ray diffraction experiments indicate that the ligand stoichiometry of the complexes formed from the reaction between zinc bis(acetate) and diethylzinc depends on the nature of the solvent (coordinating vs noncoordinating) and that the strength of the donor interaction of a coordinating solvent (THF vs pyridine) affects the nuclearity of the complex’s repeat unit in the solid state. The complexes are active catalysts for the copolymerization of cyclohexene oxide and CO2, under mild conditions. |
doi_str_mv | 10.1021/om200004a |
format | article |
fullrecord | <record><control><sourceid>acs</sourceid><recordid>TN_cdi_acs_journals_10_1021_om200004a</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>b915682593</sourcerecordid><originalsourceid>FETCH-LOGICAL-a185t-4a5b6841d6ef49cf6d3609173c0506b12b20d02d722dc523e5faa59e06d288e83</originalsourceid><addsrcrecordid>eNo9UMFOwzAUixBIjMGBP8iFY9nLS5N2x6mUMWnSDoNzlSWvWqcuqdoMsX09YyB8sWRbtmTGHgU8C0AxCXuEM1JzxUZCISQaUnHNRoCZTjIp5S27G4bdOaIziSPWrkP7ST7yF-rIO_KWeKh53BJfx_5g46G_CGXcHttT4y2fWYomEjfe8UUc-Kzr2saa2ATPG8-LFU7KLnw1jngRutAe99Q3p4t_z25q0w708Mdj9vFavhdvyXI1XxSzZWJErmKSGrXReSqcpjqd2lo7qWEqMmlBgd4I3CA4QJchOqtQkqqNUVMC7TDPKZdj9vTba-xQ7cKh9-e1SkD1c1H1f5H8Bm3nWYg</addsrcrecordid><sourcetype>Publisher</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Solvent Dependence of the Structure of Ethylzinc Acetate and Its Application in CO2/Epoxide Copolymerization</title><source>American Chemical Society:Jisc Collections:American Chemical Society Read & Publish Agreement 2022-2024 (Reading list)</source><creator>Orchard, Katherine L ; Harris, Jonathan E ; White, Andrew J. P ; Shaffer, Milo S. P ; Williams, Charlotte K</creator><creatorcontrib>Orchard, Katherine L ; Harris, Jonathan E ; White, Andrew J. P ; Shaffer, Milo S. P ; Williams, Charlotte K</creatorcontrib><description>NMR and single-crystal X-ray diffraction experiments indicate that the ligand stoichiometry of the complexes formed from the reaction between zinc bis(acetate) and diethylzinc depends on the nature of the solvent (coordinating vs noncoordinating) and that the strength of the donor interaction of a coordinating solvent (THF vs pyridine) affects the nuclearity of the complex’s repeat unit in the solid state. The complexes are active catalysts for the copolymerization of cyclohexene oxide and CO2, under mild conditions.</description><identifier>ISSN: 0276-7333</identifier><identifier>EISSN: 1520-6041</identifier><identifier>DOI: 10.1021/om200004a</identifier><language>eng</language><publisher>American Chemical Society</publisher><ispartof>Organometallics, 2011-04, Vol.30 (8), p.2223-2229</ispartof><rights>Copyright © 2011 American Chemical Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Orchard, Katherine L</creatorcontrib><creatorcontrib>Harris, Jonathan E</creatorcontrib><creatorcontrib>White, Andrew J. P</creatorcontrib><creatorcontrib>Shaffer, Milo S. P</creatorcontrib><creatorcontrib>Williams, Charlotte K</creatorcontrib><title>Solvent Dependence of the Structure of Ethylzinc Acetate and Its Application in CO2/Epoxide Copolymerization</title><title>Organometallics</title><addtitle>Organometallics</addtitle><description>NMR and single-crystal X-ray diffraction experiments indicate that the ligand stoichiometry of the complexes formed from the reaction between zinc bis(acetate) and diethylzinc depends on the nature of the solvent (coordinating vs noncoordinating) and that the strength of the donor interaction of a coordinating solvent (THF vs pyridine) affects the nuclearity of the complex’s repeat unit in the solid state. The complexes are active catalysts for the copolymerization of cyclohexene oxide and CO2, under mild conditions.</description><issn>0276-7333</issn><issn>1520-6041</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNo9UMFOwzAUixBIjMGBP8iFY9nLS5N2x6mUMWnSDoNzlSWvWqcuqdoMsX09YyB8sWRbtmTGHgU8C0AxCXuEM1JzxUZCISQaUnHNRoCZTjIp5S27G4bdOaIziSPWrkP7ST7yF-rIO_KWeKh53BJfx_5g46G_CGXcHttT4y2fWYomEjfe8UUc-Kzr2saa2ATPG8-LFU7KLnw1jngRutAe99Q3p4t_z25q0w708Mdj9vFavhdvyXI1XxSzZWJErmKSGrXReSqcpjqd2lo7qWEqMmlBgd4I3CA4QJchOqtQkqqNUVMC7TDPKZdj9vTba-xQ7cKh9-e1SkD1c1H1f5H8Bm3nWYg</recordid><startdate>20110425</startdate><enddate>20110425</enddate><creator>Orchard, Katherine L</creator><creator>Harris, Jonathan E</creator><creator>White, Andrew J. P</creator><creator>Shaffer, Milo S. P</creator><creator>Williams, Charlotte K</creator><general>American Chemical Society</general><scope/></search><sort><creationdate>20110425</creationdate><title>Solvent Dependence of the Structure of Ethylzinc Acetate and Its Application in CO2/Epoxide Copolymerization</title><author>Orchard, Katherine L ; Harris, Jonathan E ; White, Andrew J. P ; Shaffer, Milo S. P ; Williams, Charlotte K</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a185t-4a5b6841d6ef49cf6d3609173c0506b12b20d02d722dc523e5faa59e06d288e83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Orchard, Katherine L</creatorcontrib><creatorcontrib>Harris, Jonathan E</creatorcontrib><creatorcontrib>White, Andrew J. P</creatorcontrib><creatorcontrib>Shaffer, Milo S. P</creatorcontrib><creatorcontrib>Williams, Charlotte K</creatorcontrib><jtitle>Organometallics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Orchard, Katherine L</au><au>Harris, Jonathan E</au><au>White, Andrew J. P</au><au>Shaffer, Milo S. P</au><au>Williams, Charlotte K</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Solvent Dependence of the Structure of Ethylzinc Acetate and Its Application in CO2/Epoxide Copolymerization</atitle><jtitle>Organometallics</jtitle><addtitle>Organometallics</addtitle><date>2011-04-25</date><risdate>2011</risdate><volume>30</volume><issue>8</issue><spage>2223</spage><epage>2229</epage><pages>2223-2229</pages><issn>0276-7333</issn><eissn>1520-6041</eissn><abstract>NMR and single-crystal X-ray diffraction experiments indicate that the ligand stoichiometry of the complexes formed from the reaction between zinc bis(acetate) and diethylzinc depends on the nature of the solvent (coordinating vs noncoordinating) and that the strength of the donor interaction of a coordinating solvent (THF vs pyridine) affects the nuclearity of the complex’s repeat unit in the solid state. The complexes are active catalysts for the copolymerization of cyclohexene oxide and CO2, under mild conditions.</abstract><pub>American Chemical Society</pub><doi>10.1021/om200004a</doi><tpages>7</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0276-7333 |
ispartof | Organometallics, 2011-04, Vol.30 (8), p.2223-2229 |
issn | 0276-7333 1520-6041 |
language | eng |
recordid | cdi_acs_journals_10_1021_om200004a |
source | American Chemical Society:Jisc Collections:American Chemical Society Read & Publish Agreement 2022-2024 (Reading list) |
title | Solvent Dependence of the Structure of Ethylzinc Acetate and Its Application in CO2/Epoxide Copolymerization |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-02T05%3A31%3A29IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-acs&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Solvent%20Dependence%20of%20the%20Structure%20of%20Ethylzinc%20Acetate%20and%20Its%20Application%20in%20CO2/Epoxide%20Copolymerization&rft.jtitle=Organometallics&rft.au=Orchard,%20Katherine%20L&rft.date=2011-04-25&rft.volume=30&rft.issue=8&rft.spage=2223&rft.epage=2229&rft.pages=2223-2229&rft.issn=0276-7333&rft.eissn=1520-6041&rft_id=info:doi/10.1021/om200004a&rft_dat=%3Cacs%3Eb915682593%3C/acs%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-a185t-4a5b6841d6ef49cf6d3609173c0506b12b20d02d722dc523e5faa59e06d288e83%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true |