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Synthesis, LIFDI Mass Spectrometry and Reactivity of Triacyl‐Germenolates
The synthesis of stable triacylgermenolates 3 a,b was achieved by using a multiple silyl ion methodology. The formation of these new germenolates was confirmed by NMR spectroscopy and UV‐Vis measurements. Moreover, for the triacylgermenolates 2 and 3 a LIFDI mass spectrometry to characterize these n...
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Published in: | European journal of inorganic chemistry 2021-08, Vol.2021 (30), p.3091-3096 |
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container_title | European journal of inorganic chemistry |
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creator | Drusgala, Manfred Linden, Mathias H. Knoechl, Andreas Torvisco, Ana Fischer, Roland C. Bernhard Linden, H. Haas, Michael |
description | The synthesis of stable triacylgermenolates 3 a,b was achieved by using a multiple silyl ion methodology. The formation of these new germenolates was confirmed by NMR spectroscopy and UV‐Vis measurements. Moreover, for the triacylgermenolates 2 and 3 a LIFDI mass spectrometry to characterize these new compounds. Germenolates 3 a,b serve as a starting point for a new triaacylgermane 4 a and two octaacyldigermanes 4 c,d. The formation of these acylgermanes was confirmed by NMR spectroscopy, X‐ray crystallography, UV‐Vis measurements and mass spectrometry. The UV‐Vis absorption spectra of 4 c,d show considerably increased band intensities due to the presence of eight chromophores.
New Germenolates. A multiple silyl ion pathway was used to isolate two new germenolates. Their formation was confirmed by NMR spectroscopy, UV−Vis measurements as well as LIFDI mass spectrometry was used to exclude any radical side products. These germenolates serve as a starting point for new acylgermanes. |
doi_str_mv | 10.1002/ejic.202100441 |
format | article |
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New Germenolates. A multiple silyl ion pathway was used to isolate two new germenolates. Their formation was confirmed by NMR spectroscopy, UV−Vis measurements as well as LIFDI mass spectrometry was used to exclude any radical side products. These germenolates serve as a starting point for new acylgermanes.</description><identifier>ISSN: 1434-1948</identifier><identifier>EISSN: 1099-0682</identifier><identifier>DOI: 10.1002/ejic.202100441</identifier><language>eng</language><publisher>Weinheim: Wiley Subscription Services, Inc</publisher><subject>Absorption spectra ; Acylgermanes ; Chromophores ; Crystallography ; Germenolates ; Group tolerance ; Inorganic chemistry ; Ions ; Mass spectrometry ; NMR spectroscopy ; Photoinitiator ; Scientific imaging ; Spectroscopic analysis ; Synthesis</subject><ispartof>European journal of inorganic chemistry, 2021-08, Vol.2021 (30), p.3091-3096</ispartof><rights>2021 The Authors. European Journal of Inorganic Chemistry published by Wiley-VCH GmbH</rights><rights>2021. This article is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3571-254cae4c84766240146e1194d8fba14550bcbfe03214bf1a0d894630829579fa3</citedby><cites>FETCH-LOGICAL-c3571-254cae4c84766240146e1194d8fba14550bcbfe03214bf1a0d894630829579fa3</cites><orcidid>0000-0002-9213-940X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids></links><search><creatorcontrib>Drusgala, Manfred</creatorcontrib><creatorcontrib>Linden, Mathias H.</creatorcontrib><creatorcontrib>Knoechl, Andreas</creatorcontrib><creatorcontrib>Torvisco, Ana</creatorcontrib><creatorcontrib>Fischer, Roland C.</creatorcontrib><creatorcontrib>Bernhard Linden, H.</creatorcontrib><creatorcontrib>Haas, Michael</creatorcontrib><title>Synthesis, LIFDI Mass Spectrometry and Reactivity of Triacyl‐Germenolates</title><title>European journal of inorganic chemistry</title><description>The synthesis of stable triacylgermenolates 3 a,b was achieved by using a multiple silyl ion methodology. The formation of these new germenolates was confirmed by NMR spectroscopy and UV‐Vis measurements. Moreover, for the triacylgermenolates 2 and 3 a LIFDI mass spectrometry to characterize these new compounds. Germenolates 3 a,b serve as a starting point for a new triaacylgermane 4 a and two octaacyldigermanes 4 c,d. The formation of these acylgermanes was confirmed by NMR spectroscopy, X‐ray crystallography, UV‐Vis measurements and mass spectrometry. The UV‐Vis absorption spectra of 4 c,d show considerably increased band intensities due to the presence of eight chromophores.
New Germenolates. A multiple silyl ion pathway was used to isolate two new germenolates. Their formation was confirmed by NMR spectroscopy, UV−Vis measurements as well as LIFDI mass spectrometry was used to exclude any radical side products. These germenolates serve as a starting point for new acylgermanes.</description><subject>Absorption spectra</subject><subject>Acylgermanes</subject><subject>Chromophores</subject><subject>Crystallography</subject><subject>Germenolates</subject><subject>Group tolerance</subject><subject>Inorganic chemistry</subject><subject>Ions</subject><subject>Mass spectrometry</subject><subject>NMR spectroscopy</subject><subject>Photoinitiator</subject><subject>Scientific imaging</subject><subject>Spectroscopic analysis</subject><subject>Synthesis</subject><issn>1434-1948</issn><issn>1099-0682</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><recordid>eNqFkM9Kw0AQhxdRsFavngNeTZz9l2SPUtsarQi2npfNdoIpaVJ3UyU3H8Fn9ElMqejR08zA75sZPkLOKUQUgF3hqrQRA9YPQtADMqCgVAhxyg77XnARUiXSY3Li_QoAOPB4QO7nXd2-oC_9ZTDLJjdZ8GC8D-YbtK1r1ti6LjD1MnhCY9vyrWy7oCmChSuN7aqvj88pujXWTWVa9KfkqDCVx7OfOiTPk_FidBvOHqfZ6HoWWi4TGjIprEFhU5HEMRNARYy0f22ZFrmhQkrIbV4gcEZFXlADy1SJmEPKlExUYfiQXOz3blzzukXf6lWzdXV_UjMZc54kUkGfivYp6xrvHRZ648q1cZ2moHfC9E6Y_hXWA2oPvJcVdv-k9fguG_2x36ZZbpQ</recordid><startdate>20210813</startdate><enddate>20210813</enddate><creator>Drusgala, Manfred</creator><creator>Linden, Mathias H.</creator><creator>Knoechl, Andreas</creator><creator>Torvisco, Ana</creator><creator>Fischer, Roland C.</creator><creator>Bernhard Linden, H.</creator><creator>Haas, Michael</creator><general>Wiley Subscription Services, Inc</general><scope>24P</scope><scope>WIN</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope><orcidid>https://orcid.org/0000-0002-9213-940X</orcidid></search><sort><creationdate>20210813</creationdate><title>Synthesis, LIFDI Mass Spectrometry and Reactivity of Triacyl‐Germenolates</title><author>Drusgala, Manfred ; Linden, Mathias H. ; Knoechl, Andreas ; Torvisco, Ana ; Fischer, Roland C. ; Bernhard Linden, H. ; Haas, Michael</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3571-254cae4c84766240146e1194d8fba14550bcbfe03214bf1a0d894630829579fa3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Absorption spectra</topic><topic>Acylgermanes</topic><topic>Chromophores</topic><topic>Crystallography</topic><topic>Germenolates</topic><topic>Group tolerance</topic><topic>Inorganic chemistry</topic><topic>Ions</topic><topic>Mass spectrometry</topic><topic>NMR spectroscopy</topic><topic>Photoinitiator</topic><topic>Scientific imaging</topic><topic>Spectroscopic analysis</topic><topic>Synthesis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Drusgala, Manfred</creatorcontrib><creatorcontrib>Linden, Mathias H.</creatorcontrib><creatorcontrib>Knoechl, Andreas</creatorcontrib><creatorcontrib>Torvisco, Ana</creatorcontrib><creatorcontrib>Fischer, Roland C.</creatorcontrib><creatorcontrib>Bernhard Linden, H.</creatorcontrib><creatorcontrib>Haas, Michael</creatorcontrib><collection>Wiley Open Access Journals</collection><collection>Wiley-Blackwell Open Access Backfiles</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>European journal of inorganic chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Drusgala, Manfred</au><au>Linden, Mathias H.</au><au>Knoechl, Andreas</au><au>Torvisco, Ana</au><au>Fischer, Roland C.</au><au>Bernhard Linden, H.</au><au>Haas, Michael</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis, LIFDI Mass Spectrometry and Reactivity of Triacyl‐Germenolates</atitle><jtitle>European journal of inorganic chemistry</jtitle><date>2021-08-13</date><risdate>2021</risdate><volume>2021</volume><issue>30</issue><spage>3091</spage><epage>3096</epage><pages>3091-3096</pages><issn>1434-1948</issn><eissn>1099-0682</eissn><abstract>The synthesis of stable triacylgermenolates 3 a,b was achieved by using a multiple silyl ion methodology. 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New Germenolates. A multiple silyl ion pathway was used to isolate two new germenolates. Their formation was confirmed by NMR spectroscopy, UV−Vis measurements as well as LIFDI mass spectrometry was used to exclude any radical side products. These germenolates serve as a starting point for new acylgermanes.</abstract><cop>Weinheim</cop><pub>Wiley Subscription Services, Inc</pub><doi>10.1002/ejic.202100441</doi><tpages>6</tpages><orcidid>https://orcid.org/0000-0002-9213-940X</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Absorption spectra Acylgermanes Chromophores Crystallography Germenolates Group tolerance Inorganic chemistry Ions Mass spectrometry NMR spectroscopy Photoinitiator Scientific imaging Spectroscopic analysis Synthesis |
title | Synthesis, LIFDI Mass Spectrometry and Reactivity of Triacyl‐Germenolates |
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