Total surface areas of Group IVA organometallic compounds: Predictors of toxicity to algae and bacteria
There is a high correlation between molecular surface area (TSA) of triorganotin and triorganolead compounds and their toxicity towards a bacterium (Escherichia coli) and an alga (Selenastrum capricornutum). Parallel attempts to correlate other Group IVA organometals incorporating silicon or germani...
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Veröffentlicht in: | Applied organometallic chemistry 1991-01, Vol.5 (1), p.33-37 |
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description | There is a high correlation between molecular surface area (TSA) of triorganotin and triorganolead compounds and their toxicity towards a bacterium (Escherichia coli) and an alga (Selenastrum capricornutum). Parallel attempts to correlate other Group IVA organometals incorporating silicon or germanium were unsuccessful. It was further demonstrated, however, that a high correlation was obtainable between certain series of compounds with the same organic substituent but different metal centers involving all Group IVA elements. In both instances, the inability to obtain a quantitative structure‐activity relationship (QSAR) for all systems studied appears to be a function of the solubility of the compounds. While organotin TSA values have been found to correlate well with their toxicities toward various organisms, this study clearly suggests that this type of QSAR can be readily extended to include other organometal systems, provided that there is no solubility problem and the toxicity is a function of the hydrophobicity of the organometal compounds. |
doi_str_mv | 10.1002/aoc.590050104 |
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Parallel attempts to correlate other Group IVA organometals incorporating silicon or germanium were unsuccessful. It was further demonstrated, however, that a high correlation was obtainable between certain series of compounds with the same organic substituent but different metal centers involving all Group IVA elements. In both instances, the inability to obtain a quantitative structure‐activity relationship (QSAR) for all systems studied appears to be a function of the solubility of the compounds. While organotin TSA values have been found to correlate well with their toxicities toward various organisms, this study clearly suggests that this type of QSAR can be readily extended to include other organometal systems, provided that there is no solubility problem and the toxicity is a function of the hydrophobicity of the organometal compounds.</description><identifier>ISSN: 0268-2605</identifier><identifier>EISSN: 1099-0739</identifier><identifier>DOI: 10.1002/aoc.590050104</identifier><language>eng</language><publisher>New York: John Wiley & Sons, Ltd</publisher><subject>Escherichia coli ; Group IVA organometals ; molecular topology ; organogermanium ; organolead ; organosilicon ; Organotin ; quantitative structure-activity relationships (QSAR) ; Selenastrum capricornutum ; total surface area (TSA) ; toxicity</subject><ispartof>Applied organometallic chemistry, 1991-01, Vol.5 (1), p.33-37</ispartof><rights>Copyright © 1991 John Wiley & Sons, Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3234-76d95563f34b81bee2699221a41381bc7d2368ef8ffeb3a166909200e7054f573</citedby><cites>FETCH-LOGICAL-c3234-76d95563f34b81bee2699221a41381bc7d2368ef8ffeb3a166909200e7054f573</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.590050104$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Faoc.590050104$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids></links><search><creatorcontrib>Eng, G</creatorcontrib><creatorcontrib>Brinckman, F E</creatorcontrib><creatorcontrib>Olson, G J</creatorcontrib><creatorcontrib>Tierney, E J</creatorcontrib><creatorcontrib>Bellama, J M</creatorcontrib><title>Total surface areas of Group IVA organometallic compounds: Predictors of toxicity to algae and bacteria</title><title>Applied organometallic chemistry</title><addtitle>Appl. Organometal. Chem</addtitle><description>There is a high correlation between molecular surface area (TSA) of triorganotin and triorganolead compounds and their toxicity towards a bacterium (Escherichia coli) and an alga (Selenastrum capricornutum). Parallel attempts to correlate other Group IVA organometals incorporating silicon or germanium were unsuccessful. It was further demonstrated, however, that a high correlation was obtainable between certain series of compounds with the same organic substituent but different metal centers involving all Group IVA elements. In both instances, the inability to obtain a quantitative structure‐activity relationship (QSAR) for all systems studied appears to be a function of the solubility of the compounds. While organotin TSA values have been found to correlate well with their toxicities toward various organisms, this study clearly suggests that this type of QSAR can be readily extended to include other organometal systems, provided that there is no solubility problem and the toxicity is a function of the hydrophobicity of the organometal compounds.</description><subject>Escherichia coli</subject><subject>Group IVA organometals</subject><subject>molecular topology</subject><subject>organogermanium</subject><subject>organolead</subject><subject>organosilicon</subject><subject>Organotin</subject><subject>quantitative structure-activity relationships (QSAR)</subject><subject>Selenastrum capricornutum</subject><subject>total surface area (TSA)</subject><subject>toxicity</subject><issn>0268-2605</issn><issn>1099-0739</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1991</creationdate><recordtype>article</recordtype><recordid>eNp9kEFPAjEQhRujiYgevfcPLE7b3XbrjaAihqgH1MRL0-22ZHWhpF0i_HurEOLJ08wk33vz8hC6JDAgAPRKezMoJEABBPIj1CMgZQaCyWPUA8rLjHIoTtFZjB8AIDnJe2g-851ucVwHp43FOlgdsXd4HPx6hSevQ-zDXC_9wiasbQw2frHy62Udr_FzsHVjOh9-FZ3fNKbptmnBup3rZLascaVNZ0Ojz9GJ0220F_vZRy93t7PRfTZ9Gk9Gw2lmGGV5Jngti4Izx_KqJJW1lEtJKdE5Yek2oqaMl9aVztmKacK5BEkBrIAid4VgfZTtfE3wMQbr1Co0Cx22ioD6aUmlltShpcSLHf_VtHb7P6yGT6O_yv2nJnZ2c1Dq8Km4YKJQb49jNX14T7lvkhv7BkOsebw</recordid><startdate>199101</startdate><enddate>199101</enddate><creator>Eng, G</creator><creator>Brinckman, F E</creator><creator>Olson, G J</creator><creator>Tierney, E J</creator><creator>Bellama, J M</creator><general>John Wiley & Sons, Ltd</general><scope>BSCLL</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>199101</creationdate><title>Total surface areas of Group IVA organometallic compounds: Predictors of toxicity to algae and bacteria</title><author>Eng, G ; Brinckman, F E ; Olson, G J ; Tierney, E J ; Bellama, J M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3234-76d95563f34b81bee2699221a41381bc7d2368ef8ffeb3a166909200e7054f573</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1991</creationdate><topic>Escherichia coli</topic><topic>Group IVA organometals</topic><topic>molecular topology</topic><topic>organogermanium</topic><topic>organolead</topic><topic>organosilicon</topic><topic>Organotin</topic><topic>quantitative structure-activity relationships (QSAR)</topic><topic>Selenastrum capricornutum</topic><topic>total surface area (TSA)</topic><topic>toxicity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Eng, G</creatorcontrib><creatorcontrib>Brinckman, F E</creatorcontrib><creatorcontrib>Olson, G J</creatorcontrib><creatorcontrib>Tierney, E J</creatorcontrib><creatorcontrib>Bellama, J M</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>Eng, G</au><au>Brinckman, F E</au><au>Olson, G J</au><au>Tierney, E J</au><au>Bellama, J M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Total surface areas of Group IVA organometallic compounds: Predictors of toxicity to algae and bacteria</atitle><jtitle>Applied organometallic chemistry</jtitle><addtitle>Appl. Organometal. Chem</addtitle><date>1991-01</date><risdate>1991</risdate><volume>5</volume><issue>1</issue><spage>33</spage><epage>37</epage><pages>33-37</pages><issn>0268-2605</issn><eissn>1099-0739</eissn><abstract>There is a high correlation between molecular surface area (TSA) of triorganotin and triorganolead compounds and their toxicity towards a bacterium (Escherichia coli) and an alga (Selenastrum capricornutum). Parallel attempts to correlate other Group IVA organometals incorporating silicon or germanium were unsuccessful. It was further demonstrated, however, that a high correlation was obtainable between certain series of compounds with the same organic substituent but different metal centers involving all Group IVA elements. In both instances, the inability to obtain a quantitative structure‐activity relationship (QSAR) for all systems studied appears to be a function of the solubility of the compounds. While organotin TSA values have been found to correlate well with their toxicities toward various organisms, this study clearly suggests that this type of QSAR can be readily extended to include other organometal systems, provided that there is no solubility problem and the toxicity is a function of the hydrophobicity of the organometal compounds.</abstract><cop>New York</cop><pub>John Wiley & Sons, Ltd</pub><doi>10.1002/aoc.590050104</doi><tpages>5</tpages></addata></record> |
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subjects | Escherichia coli Group IVA organometals molecular topology organogermanium organolead organosilicon Organotin quantitative structure-activity relationships (QSAR) Selenastrum capricornutum total surface area (TSA) toxicity |
title | Total surface areas of Group IVA organometallic compounds: Predictors of toxicity to algae and bacteria |
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