Ruthenium Carbene-Based Olefin Metathesis Initiators: Catalyst Decomposition and Longevity
Thermolytic decomposition pathways were studied for several ruthenium carbene-based olefin metathesis catalysts. Substituted carbenes were found to decompose through bimolecular pathways while the unsubstituted carbene was found to decomposed unimolecularly. Implications for ring-closing metathesis...
Gespeichert in:
Veröffentlicht in: | Journal of organic chemistry 1999-09, Vol.64 (19), p.7202-7207 |
---|---|
Hauptverfasser: | , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 7207 |
---|---|
container_issue | 19 |
container_start_page | 7202 |
container_title | Journal of organic chemistry |
container_volume | 64 |
creator | Ulman, Michael Grubbs, Robert H |
description | Thermolytic decomposition pathways were studied for several ruthenium carbene-based olefin metathesis catalysts. Substituted carbenes were found to decompose through bimolecular pathways while the unsubstituted carbene was found to decomposed unimolecularly. Implications for ring-closing metathesis are discussed, and the longevity of several ruthenium-based catalysts are compared. |
doi_str_mv | 10.1021/jo9908703 |
format | Article |
fullrecord | <record><control><sourceid>acs_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1021_jo9908703</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>b200865238</sourcerecordid><originalsourceid>FETCH-LOGICAL-a361t-3e2d3a0c7dbd1c622ea3a87db53b480b8ad3c41cd4a217d31ad1b1616edeef4c3</originalsourceid><addsrcrecordid>eNpt0LlOAzEQBmALgUQIFLzBNhQUCz72Ch1sOCJtFI4gKmTN2hNwSHYj20Gko-U1eRKMglIxzWg0n35phpBDRk8Y5ex02vZ6tMip2CIdlnIaZz2abJMOpZzHgmdil-w5N6Wh0jTtkOf7pX_FxiznUQm2xgbjC3Coo9EMJ6aJhughAGdcNGiMN-Bb686-P78C9zBbOR_1UbXzRevCtm0iaHRUtc0Lvhu_2ic7E5g5PPjrXfJ4dTkub-JqdD0oz6sYRMZ8LJBrAVTlutZMZZwjCCjClIo6KWhdgBYqYUonwFmuBQPNapaxDDXiJFGiS47Xucq2zlmcyIU1c7Aryaj8_Yvc_CXYeG2N8_ixgWDfZJaLPJXj2wdZPvXHpaju5DD4o7UH5ULM0jbhkn9yfwCMxXNr</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Ruthenium Carbene-Based Olefin Metathesis Initiators: Catalyst Decomposition and Longevity</title><source>ACS Publications</source><creator>Ulman, Michael ; Grubbs, Robert H</creator><creatorcontrib>Ulman, Michael ; Grubbs, Robert H</creatorcontrib><description>Thermolytic decomposition pathways were studied for several ruthenium carbene-based olefin metathesis catalysts. Substituted carbenes were found to decompose through bimolecular pathways while the unsubstituted carbene was found to decomposed unimolecularly. Implications for ring-closing metathesis are discussed, and the longevity of several ruthenium-based catalysts are compared.</description><identifier>ISSN: 0022-3263</identifier><identifier>EISSN: 1520-6904</identifier><identifier>DOI: 10.1021/jo9908703</identifier><language>eng</language><publisher>American Chemical Society</publisher><ispartof>Journal of organic chemistry, 1999-09, Vol.64 (19), p.7202-7207</ispartof><rights>Copyright © 1999 American Chemical Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a361t-3e2d3a0c7dbd1c622ea3a87db53b480b8ad3c41cd4a217d31ad1b1616edeef4c3</citedby><cites>FETCH-LOGICAL-a361t-3e2d3a0c7dbd1c622ea3a87db53b480b8ad3c41cd4a217d31ad1b1616edeef4c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/jo9908703$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/jo9908703$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,780,784,2764,27075,27923,27924,56737,56787</link.rule.ids></links><search><creatorcontrib>Ulman, Michael</creatorcontrib><creatorcontrib>Grubbs, Robert H</creatorcontrib><title>Ruthenium Carbene-Based Olefin Metathesis Initiators: Catalyst Decomposition and Longevity</title><title>Journal of organic chemistry</title><addtitle>J. Org. Chem</addtitle><description>Thermolytic decomposition pathways were studied for several ruthenium carbene-based olefin metathesis catalysts. Substituted carbenes were found to decompose through bimolecular pathways while the unsubstituted carbene was found to decomposed unimolecularly. Implications for ring-closing metathesis are discussed, and the longevity of several ruthenium-based catalysts are compared.</description><issn>0022-3263</issn><issn>1520-6904</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><recordid>eNpt0LlOAzEQBmALgUQIFLzBNhQUCz72Ch1sOCJtFI4gKmTN2hNwSHYj20Gko-U1eRKMglIxzWg0n35phpBDRk8Y5ex02vZ6tMip2CIdlnIaZz2abJMOpZzHgmdil-w5N6Wh0jTtkOf7pX_FxiznUQm2xgbjC3Coo9EMJ6aJhughAGdcNGiMN-Bb686-P78C9zBbOR_1UbXzRevCtm0iaHRUtc0Lvhu_2ic7E5g5PPjrXfJ4dTkub-JqdD0oz6sYRMZ8LJBrAVTlutZMZZwjCCjClIo6KWhdgBYqYUonwFmuBQPNapaxDDXiJFGiS47Xucq2zlmcyIU1c7Aryaj8_Yvc_CXYeG2N8_ixgWDfZJaLPJXj2wdZPvXHpaju5DD4o7UH5ULM0jbhkn9yfwCMxXNr</recordid><startdate>19990917</startdate><enddate>19990917</enddate><creator>Ulman, Michael</creator><creator>Grubbs, Robert H</creator><general>American Chemical Society</general><scope>BSCLL</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>19990917</creationdate><title>Ruthenium Carbene-Based Olefin Metathesis Initiators: Catalyst Decomposition and Longevity</title><author>Ulman, Michael ; Grubbs, Robert H</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a361t-3e2d3a0c7dbd1c622ea3a87db53b480b8ad3c41cd4a217d31ad1b1616edeef4c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ulman, Michael</creatorcontrib><creatorcontrib>Grubbs, Robert H</creatorcontrib><collection>Istex</collection><collection>CrossRef</collection><jtitle>Journal of organic chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ulman, Michael</au><au>Grubbs, Robert H</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ruthenium Carbene-Based Olefin Metathesis Initiators: Catalyst Decomposition and Longevity</atitle><jtitle>Journal of organic chemistry</jtitle><addtitle>J. Org. Chem</addtitle><date>1999-09-17</date><risdate>1999</risdate><volume>64</volume><issue>19</issue><spage>7202</spage><epage>7207</epage><pages>7202-7207</pages><issn>0022-3263</issn><eissn>1520-6904</eissn><abstract>Thermolytic decomposition pathways were studied for several ruthenium carbene-based olefin metathesis catalysts. Substituted carbenes were found to decompose through bimolecular pathways while the unsubstituted carbene was found to decomposed unimolecularly. Implications for ring-closing metathesis are discussed, and the longevity of several ruthenium-based catalysts are compared.</abstract><pub>American Chemical Society</pub><doi>10.1021/jo9908703</doi><tpages>6</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0022-3263 |
ispartof | Journal of organic chemistry, 1999-09, Vol.64 (19), p.7202-7207 |
issn | 0022-3263 1520-6904 |
language | eng |
recordid | cdi_crossref_primary_10_1021_jo9908703 |
source | ACS Publications |
title | Ruthenium Carbene-Based Olefin Metathesis Initiators: Catalyst Decomposition and Longevity |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-08T21%3A09%3A07IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-acs_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Ruthenium%20Carbene-Based%20Olefin%20Metathesis%20Initiators:%E2%80%89%20Catalyst%20Decomposition%20and%20Longevity&rft.jtitle=Journal%20of%20organic%20chemistry&rft.au=Ulman,%20Michael&rft.date=1999-09-17&rft.volume=64&rft.issue=19&rft.spage=7202&rft.epage=7207&rft.pages=7202-7207&rft.issn=0022-3263&rft.eissn=1520-6904&rft_id=info:doi/10.1021/jo9908703&rft_dat=%3Cacs_cross%3Eb200865238%3C/acs_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true |