Mass spectrometry studies of organometallic compounds: Part 1. Compounds of general formula PhnGeCl4-n

The mass spectra of organogermanium compounds of the type PhnGeCl4‐n (where n = 1–4) were investigated. Positive and negative ion spectra of these compounds were recorded using conventional electron impact (EI) conditions. In common with the analogous tetra‐alkyltin compound, Ph4Ge produced no negat...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Applied organometallic chemistry 1995-11, Vol.9 (7), p.609-615
Hauptverfasser: Ostah, N., Lawson, G.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 615
container_issue 7
container_start_page 609
container_title Applied organometallic chemistry
container_volume 9
creator Ostah, N.
Lawson, G.
description The mass spectra of organogermanium compounds of the type PhnGeCl4‐n (where n = 1–4) were investigated. Positive and negative ion spectra of these compounds were recorded using conventional electron impact (EI) conditions. In common with the analogous tetra‐alkyltin compound, Ph4Ge produced no negative ion spectra under these conditions. Tandem mass spectrometry (MS–MS) was used to deduce fragmetation reaction pathways for these compounds. In the case of PhGeCl3, collision‐induced dissociation studies were extended to examine the ion–molecule reactions under relatively high reactant pressures of methanol and/or water vapour in the collision cell of the MS–MS instrument.
doi_str_mv 10.1002/aoc.590090716
format Article
fullrecord <record><control><sourceid>wiley_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1002_aoc_590090716</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>AOC590090716</sourcerecordid><originalsourceid>FETCH-LOGICAL-c2386-23d71f2e8160875a9618756ad5324f4420b8950f89b4e37e6d45aebb12c2b1d03</originalsourceid><addsrcrecordid>eNp9kFFLwzAUhYMoOKePvucPdN4kbdL6NqpuytwGKj6GtE1mNW1G0qH793ZMh08-HTh859zLQeiSwIgA0CvlylGSAWQgCD9CAwJZFoFg2TEaAOVpRDkkp-gshHfoKU7iATKPKgQc1rrsvGt057c4dJuq1gE7g51fqXZnK2vrEpeuWbtNW4VrvFS-w2SE819rh690q72y2DjfbKzCy7d2onMbR-05OjHKBn3xo0P0cnf7nE-j2WJyn49nUUlZyiPKKkEM1SnhkIpE9T_2wlWVMBqbOKZQpFkCJs2KWDOheRUnShcFoSUtSAVsiKJ9b-ldCF4bufZ1o_xWEpC7kWQ_kjyM1PNiz3_WVm__h-V4kf9N_lyqQ6e_DknlPyQXTCTydT6RZMpvHuZsKZ_YN_bkec4</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Mass spectrometry studies of organometallic compounds: Part 1. Compounds of general formula PhnGeCl4-n</title><source>Access via Wiley Online Library</source><creator>Ostah, N. ; Lawson, G.</creator><creatorcontrib>Ostah, N. ; Lawson, G.</creatorcontrib><description>The mass spectra of organogermanium compounds of the type PhnGeCl4‐n (where n = 1–4) were investigated. Positive and negative ion spectra of these compounds were recorded using conventional electron impact (EI) conditions. In common with the analogous tetra‐alkyltin compound, Ph4Ge produced no negative ion spectra under these conditions. Tandem mass spectrometry (MS–MS) was used to deduce fragmetation reaction pathways for these compounds. In the case of PhGeCl3, collision‐induced dissociation studies were extended to examine the ion–molecule reactions under relatively high reactant pressures of methanol and/or water vapour in the collision cell of the MS–MS instrument.</description><identifier>ISSN: 0268-2605</identifier><identifier>EISSN: 1099-0739</identifier><identifier>DOI: 10.1002/aoc.590090716</identifier><language>eng</language><publisher>West Sussex: John Wiley &amp; Sons, Ltd</publisher><subject>ion-molecule reaction ; organogermanium compounds ; tandem mass Spectrometry</subject><ispartof>Applied organometallic chemistry, 1995-11, Vol.9 (7), p.609-615</ispartof><rights>Copyright © 1995 John Wiley &amp; Sons, Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2386-23d71f2e8160875a9618756ad5324f4420b8950f89b4e37e6d45aebb12c2b1d03</citedby><cites>FETCH-LOGICAL-c2386-23d71f2e8160875a9618756ad5324f4420b8950f89b4e37e6d45aebb12c2b1d03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Faoc.590090716$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Faoc.590090716$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids></links><search><creatorcontrib>Ostah, N.</creatorcontrib><creatorcontrib>Lawson, G.</creatorcontrib><title>Mass spectrometry studies of organometallic compounds: Part 1. Compounds of general formula PhnGeCl4-n</title><title>Applied organometallic chemistry</title><addtitle>Appl. Organometal. Chem</addtitle><description>The mass spectra of organogermanium compounds of the type PhnGeCl4‐n (where n = 1–4) were investigated. Positive and negative ion spectra of these compounds were recorded using conventional electron impact (EI) conditions. In common with the analogous tetra‐alkyltin compound, Ph4Ge produced no negative ion spectra under these conditions. Tandem mass spectrometry (MS–MS) was used to deduce fragmetation reaction pathways for these compounds. In the case of PhGeCl3, collision‐induced dissociation studies were extended to examine the ion–molecule reactions under relatively high reactant pressures of methanol and/or water vapour in the collision cell of the MS–MS instrument.</description><subject>ion-molecule reaction</subject><subject>organogermanium compounds</subject><subject>tandem mass Spectrometry</subject><issn>0268-2605</issn><issn>1099-0739</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1995</creationdate><recordtype>article</recordtype><recordid>eNp9kFFLwzAUhYMoOKePvucPdN4kbdL6NqpuytwGKj6GtE1mNW1G0qH793ZMh08-HTh859zLQeiSwIgA0CvlylGSAWQgCD9CAwJZFoFg2TEaAOVpRDkkp-gshHfoKU7iATKPKgQc1rrsvGt057c4dJuq1gE7g51fqXZnK2vrEpeuWbtNW4VrvFS-w2SE819rh690q72y2DjfbKzCy7d2onMbR-05OjHKBn3xo0P0cnf7nE-j2WJyn49nUUlZyiPKKkEM1SnhkIpE9T_2wlWVMBqbOKZQpFkCJs2KWDOheRUnShcFoSUtSAVsiKJ9b-ldCF4bufZ1o_xWEpC7kWQ_kjyM1PNiz3_WVm__h-V4kf9N_lyqQ6e_DknlPyQXTCTydT6RZMpvHuZsKZ_YN_bkec4</recordid><startdate>199511</startdate><enddate>199511</enddate><creator>Ostah, N.</creator><creator>Lawson, G.</creator><general>John Wiley &amp; Sons, Ltd</general><scope>BSCLL</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>199511</creationdate><title>Mass spectrometry studies of organometallic compounds: Part 1. Compounds of general formula PhnGeCl4-n</title><author>Ostah, N. ; Lawson, G.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2386-23d71f2e8160875a9618756ad5324f4420b8950f89b4e37e6d45aebb12c2b1d03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1995</creationdate><topic>ion-molecule reaction</topic><topic>organogermanium compounds</topic><topic>tandem mass Spectrometry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ostah, N.</creatorcontrib><creatorcontrib>Lawson, G.</creatorcontrib><collection>Istex</collection><collection>CrossRef</collection><jtitle>Applied organometallic chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ostah, N.</au><au>Lawson, G.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mass spectrometry studies of organometallic compounds: Part 1. Compounds of general formula PhnGeCl4-n</atitle><jtitle>Applied organometallic chemistry</jtitle><addtitle>Appl. Organometal. Chem</addtitle><date>1995-11</date><risdate>1995</risdate><volume>9</volume><issue>7</issue><spage>609</spage><epage>615</epage><pages>609-615</pages><issn>0268-2605</issn><eissn>1099-0739</eissn><abstract>The mass spectra of organogermanium compounds of the type PhnGeCl4‐n (where n = 1–4) were investigated. Positive and negative ion spectra of these compounds were recorded using conventional electron impact (EI) conditions. In common with the analogous tetra‐alkyltin compound, Ph4Ge produced no negative ion spectra under these conditions. Tandem mass spectrometry (MS–MS) was used to deduce fragmetation reaction pathways for these compounds. In the case of PhGeCl3, collision‐induced dissociation studies were extended to examine the ion–molecule reactions under relatively high reactant pressures of methanol and/or water vapour in the collision cell of the MS–MS instrument.</abstract><cop>West Sussex</cop><pub>John Wiley &amp; Sons, Ltd</pub><doi>10.1002/aoc.590090716</doi><tpages>7</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0268-2605
ispartof Applied organometallic chemistry, 1995-11, Vol.9 (7), p.609-615
issn 0268-2605
1099-0739
language eng
recordid cdi_crossref_primary_10_1002_aoc_590090716
source Access via Wiley Online Library
subjects ion-molecule reaction
organogermanium compounds
tandem mass Spectrometry
title Mass spectrometry studies of organometallic compounds: Part 1. Compounds of general formula PhnGeCl4-n
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-28T17%3A07%3A51IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-wiley_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Mass%20spectrometry%20studies%20of%20organometallic%20compounds:%20Part%201.%20Compounds%20of%20general%20formula%20PhnGeCl4-n&rft.jtitle=Applied%20organometallic%20chemistry&rft.au=Ostah,%20N.&rft.date=1995-11&rft.volume=9&rft.issue=7&rft.spage=609&rft.epage=615&rft.pages=609-615&rft.issn=0268-2605&rft.eissn=1099-0739&rft_id=info:doi/10.1002/aoc.590090716&rft_dat=%3Cwiley_cross%3EAOC590090716%3C/wiley_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