Loading…
Organometallic Chemistry in Homogeneous Catalysis
Many reactions catalyzed by soluble transition metal compounds proceed by way of organometallic intermediates, even though the original catalyst may be a simple salt. This generality is illustrated for three industrial syntheses of acetic acid that use homogeneous catalysts. Some developments in org...
Saved in:
Published in: | Science (American Association for the Advancement of Science) 1980-06, Vol.208 (4449), p.1221-1224 |
---|---|
Main Author: | |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c421t-89cde92a795c2898e29e707291c1f2c62227426e2fe8937e363c0ee379b4b5e03 |
---|---|
cites | cdi_FETCH-LOGICAL-c421t-89cde92a795c2898e29e707291c1f2c62227426e2fe8937e363c0ee379b4b5e03 |
container_end_page | 1224 |
container_issue | 4449 |
container_start_page | 1221 |
container_title | Science (American Association for the Advancement of Science) |
container_volume | 208 |
creator | Parshall, George W. |
description | Many reactions catalyzed by soluble transition metal compounds proceed by way of organometallic intermediates, even though the original catalyst may be a simple salt. This generality is illustrated for three industrial syntheses of acetic acid that use homogeneous catalysts. Some developments in organometallic chemistry that may extend the utility of homogeneous catalysis are photoactivation of catalysts and the recognition of the importance of metallacyclic intermediates. |
doi_str_mv | 10.1126/science.208.4449.1221 |
format | article |
fullrecord | <record><control><sourceid>gale_proqu</sourceid><recordid>TN_cdi_proquest_miscellaneous_733236680</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A1612392</galeid><jstor_id>1683967</jstor_id><sourcerecordid>A1612392</sourcerecordid><originalsourceid>FETCH-LOGICAL-c421t-89cde92a795c2898e29e707291c1f2c62227426e2fe8937e363c0ee379b4b5e03</originalsourceid><addsrcrecordid>eNpFkE1Lw0AURQdRbK3-A5XsXEjizJtkPpYlqBUK3eh6SKcvMSXJ1EwK9t-bmEBXb3HPfVwOIQ-MRoyBePG2xMZiBFRFcRzriAGwCzJnVCehBsovyZxSLkJFZTIjN97vKe0zza_JjEnFqdR8TtimLbLG1dhlVVXaIP3GuvRdewrKJli52hXYoDv6IM164uRLf0uu8qzyeDfdBfl6e_1MV-F68_6RLtehjYF1odJ2hxoyqRMLSisEjZJK0MyyHKwAABmDQMhRaS6RC24pIpd6G28TpHxBnsa_h9b9HNF3ph9msaqy_0FGcg5cCDWQzyNZZBWasrGu6fC3s66qsEDTr0o3ZskEA66hp5ORtq3zvsXcHNqyztqTYdQMas2k1vRqzaDWDGr73uO057itcXduTS574H4E9r5z7TkXimsh-R_65X4q</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>733236680</pqid></control><display><type>article</type><title>Organometallic Chemistry in Homogeneous Catalysis</title><source>Science Online科学在线</source><creator>Parshall, George W.</creator><creatorcontrib>Parshall, George W.</creatorcontrib><description>Many reactions catalyzed by soluble transition metal compounds proceed by way of organometallic intermediates, even though the original catalyst may be a simple salt. This generality is illustrated for three industrial syntheses of acetic acid that use homogeneous catalysts. Some developments in organometallic chemistry that may extend the utility of homogeneous catalysis are photoactivation of catalysts and the recognition of the importance of metallacyclic intermediates.</description><identifier>ISSN: 0036-8075</identifier><identifier>EISSN: 1095-9203</identifier><identifier>DOI: 10.1126/science.208.4449.1221</identifier><identifier>PMID: 17830793</identifier><language>eng</language><publisher>United States: The American Association for the Advancement of Science</publisher><subject>Acetates ; Alkenes ; Alkynes ; Catalysis ; Catalysts ; Coordination chemistry ; Iodides ; Metal ions ; Organometallic compounds ; Oxidation ; Palladium</subject><ispartof>Science (American Association for the Advancement of Science), 1980-06, Vol.208 (4449), p.1221-1224</ispartof><rights>Copyright 1980 The American Association for the Advancement of Science</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c421t-89cde92a795c2898e29e707291c1f2c62227426e2fe8937e363c0ee379b4b5e03</citedby><cites>FETCH-LOGICAL-c421t-89cde92a795c2898e29e707291c1f2c62227426e2fe8937e363c0ee379b4b5e03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,2884,2885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17830793$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Parshall, George W.</creatorcontrib><title>Organometallic Chemistry in Homogeneous Catalysis</title><title>Science (American Association for the Advancement of Science)</title><addtitle>Science</addtitle><description>Many reactions catalyzed by soluble transition metal compounds proceed by way of organometallic intermediates, even though the original catalyst may be a simple salt. This generality is illustrated for three industrial syntheses of acetic acid that use homogeneous catalysts. Some developments in organometallic chemistry that may extend the utility of homogeneous catalysis are photoactivation of catalysts and the recognition of the importance of metallacyclic intermediates.</description><subject>Acetates</subject><subject>Alkenes</subject><subject>Alkynes</subject><subject>Catalysis</subject><subject>Catalysts</subject><subject>Coordination chemistry</subject><subject>Iodides</subject><subject>Metal ions</subject><subject>Organometallic compounds</subject><subject>Oxidation</subject><subject>Palladium</subject><issn>0036-8075</issn><issn>1095-9203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1980</creationdate><recordtype>article</recordtype><recordid>eNpFkE1Lw0AURQdRbK3-A5XsXEjizJtkPpYlqBUK3eh6SKcvMSXJ1EwK9t-bmEBXb3HPfVwOIQ-MRoyBePG2xMZiBFRFcRzriAGwCzJnVCehBsovyZxSLkJFZTIjN97vKe0zza_JjEnFqdR8TtimLbLG1dhlVVXaIP3GuvRdewrKJli52hXYoDv6IM164uRLf0uu8qzyeDfdBfl6e_1MV-F68_6RLtehjYF1odJ2hxoyqRMLSisEjZJK0MyyHKwAABmDQMhRaS6RC24pIpd6G28TpHxBnsa_h9b9HNF3ph9msaqy_0FGcg5cCDWQzyNZZBWasrGu6fC3s66qsEDTr0o3ZskEA66hp5ORtq3zvsXcHNqyztqTYdQMas2k1vRqzaDWDGr73uO057itcXduTS574H4E9r5z7TkXimsh-R_65X4q</recordid><startdate>19800613</startdate><enddate>19800613</enddate><creator>Parshall, George W.</creator><general>The American Association for the Advancement of Science</general><general>American Association for the Advancement of Science</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>19800613</creationdate><title>Organometallic Chemistry in Homogeneous Catalysis</title><author>Parshall, George W.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c421t-89cde92a795c2898e29e707291c1f2c62227426e2fe8937e363c0ee379b4b5e03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1980</creationdate><topic>Acetates</topic><topic>Alkenes</topic><topic>Alkynes</topic><topic>Catalysis</topic><topic>Catalysts</topic><topic>Coordination chemistry</topic><topic>Iodides</topic><topic>Metal ions</topic><topic>Organometallic compounds</topic><topic>Oxidation</topic><topic>Palladium</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Parshall, George W.</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Science (American Association for the Advancement of Science)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Parshall, George W.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Organometallic Chemistry in Homogeneous Catalysis</atitle><jtitle>Science (American Association for the Advancement of Science)</jtitle><addtitle>Science</addtitle><date>1980-06-13</date><risdate>1980</risdate><volume>208</volume><issue>4449</issue><spage>1221</spage><epage>1224</epage><pages>1221-1224</pages><issn>0036-8075</issn><eissn>1095-9203</eissn><abstract>Many reactions catalyzed by soluble transition metal compounds proceed by way of organometallic intermediates, even though the original catalyst may be a simple salt. This generality is illustrated for three industrial syntheses of acetic acid that use homogeneous catalysts. Some developments in organometallic chemistry that may extend the utility of homogeneous catalysis are photoactivation of catalysts and the recognition of the importance of metallacyclic intermediates.</abstract><cop>United States</cop><pub>The American Association for the Advancement of Science</pub><pmid>17830793</pmid><doi>10.1126/science.208.4449.1221</doi><tpages>4</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0036-8075 |
ispartof | Science (American Association for the Advancement of Science), 1980-06, Vol.208 (4449), p.1221-1224 |
issn | 0036-8075 1095-9203 |
language | eng |
recordid | cdi_proquest_miscellaneous_733236680 |
source | Science Online科学在线 |
subjects | Acetates Alkenes Alkynes Catalysis Catalysts Coordination chemistry Iodides Metal ions Organometallic compounds Oxidation Palladium |
title | Organometallic Chemistry in Homogeneous Catalysis |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-05T02%3A10%3A34IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_proqu&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Organometallic%20Chemistry%20in%20Homogeneous%20Catalysis&rft.jtitle=Science%20(American%20Association%20for%20the%20Advancement%20of%20Science)&rft.au=Parshall,%20George%20W.&rft.date=1980-06-13&rft.volume=208&rft.issue=4449&rft.spage=1221&rft.epage=1224&rft.pages=1221-1224&rft.issn=0036-8075&rft.eissn=1095-9203&rft_id=info:doi/10.1126/science.208.4449.1221&rft_dat=%3Cgale_proqu%3EA1612392%3C/gale_proqu%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c421t-89cde92a795c2898e29e707291c1f2c62227426e2fe8937e363c0ee379b4b5e03%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=733236680&rft_id=info:pmid/17830793&rft_galeid=A1612392&rft_jstor_id=1683967&rfr_iscdi=true |