The synthesis and characterisation of C -triorganometallated (metal=Sn, Si) bis-(thienyl)- and bis-(pyrazolyl)alkanes, including the crystal structure of [(Ph3Sn)C3N2]2CH2
Identifieur interne : 001347 ( Istex/Corpus ); précédent : 001346; suivant : 001348The synthesis and characterisation of C -triorganometallated (metal=Sn, Si) bis-(thienyl)- and bis-(pyrazolyl)alkanes, including the crystal structure of [(Ph3Sn)C3N2]2CH2
Auteurs : Michael S. Hill ; Mary F. Mahon ; John M. G. Mcginley ; Kieran C. MolloySource :
- Polyhedron [ 0277-5387 ] ; 2001.
English descriptors
- KwdEn :
- Teeft :
- Anal, Anion formation, Asymmetric unit, Bond angles, Bond lengths, Bond polarities, Buli, Calc, Chem, Chemical shifts, Colourless, Computer program, Crystal structure, Derivative, Diethyl, Diethyl ether, Elsevier science, Ether, Hexane, Lithiation, Mmol, Mossbauer, Organomet, Perkin trans, Petroleum ether, Phenyl groups, Phenyl rings, Polyhedron, Previous work, Pyrazole, Room temperature, Subsequent substitution, Tetrahedral geometry, Tributyltin chloride, Trimethylsilyl chloride, Trimethyltin chloride, Triphenyltin chloride, Unresolved, Vacuo, Vacuo removal, Vacuum distillation, White suspension, Yellow solution, Yellow suspension.
Abstract
Abstract: C-organostannyl- and organosilyl-derivatives of 2-(thien-2-ylmethyl)thiophene and 1-[(1H-pyrazol-1-yl)methyl]-1H-pyrazole have been synthesised and characterised spectroscopically. Lithiation and subsequent substitution by R3M takes place at the 5,5′ positions for both bis-heterocycles, and this is confirmed by the X-ray structure of 1,1′-[5,5′-(Ph3Sn)C3N2]2CH2.
C-organostannyl- and organosilyl-derivatives of 2-(thien-2-ylmethyl)thiophene and 1-[(1H-pyrazol-1-yl)methyl]-1H-pyrazole have been synthesised. Substitution by R3M takes place at the 5,5′ positions for both bis-heterocycles and this is confirmed by the X-ray structure of 1,1′-(5,5′-(Ph3Sn)C3N2]2CH2.loc1
Url:
DOI: 10.1016/S0277-5387(01)00799-9
Links to Exploration step
ISTEX:2C9D4E77B75296C010C26C236FE17F62B7ABA8ECLe document en format XML
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Hill</name><affiliation><mods:affiliation>Department of Chemistry, University of Bath, Claverton Down, Bath BA2 7AY, UK</mods:affiliation></affiliation></author><author><name sortKey="Mahon, Mary F" sort="Mahon, Mary F" uniqKey="Mahon M" first="Mary F." last="Mahon">Mary F. Mahon</name><affiliation><mods:affiliation>Department of Chemistry, University of Bath, Claverton Down, Bath BA2 7AY, UK</mods:affiliation></affiliation></author><author><name sortKey="Mcginley, John M G" sort="Mcginley, John M G" uniqKey="Mcginley J" first="John M. G." last="Mcginley">John M. G. Mcginley</name><affiliation><mods:affiliation>Department of Chemistry, University of Bath, Claverton Down, Bath BA2 7AY, UK</mods:affiliation></affiliation></author><author><name sortKey="Molloy, Kieran C" sort="Molloy, Kieran C" uniqKey="Molloy K" first="Kieran C." last="Molloy">Kieran C. Molloy</name><affiliation><mods:affiliation>Department of Chemistry, University of Bath, Claverton Down, Bath BA2 7AY, UK</mods:affiliation></affiliation><affiliation><mods:affiliation>E-mail: chskcm@bath.ac.uk</mods:affiliation></affiliation></author></analytic><monogr></monogr><series><title level="j">Polyhedron</title><title level="j" type="abbrev">POLY</title><idno type="ISSN">0277-5387</idno><imprint><publisher>ELSEVIER</publisher><date type="published" when="2001">2001</date><biblScope unit="volume">20</biblScope><biblScope unit="issue">15–16</biblScope><biblScope unit="page" from="1995">1995</biblScope><biblScope unit="page" to="2002">2002</biblScope></imprint><idno type="ISSN">0277-5387</idno></series></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0277-5387</idno></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Mössbauer</term><term>Organosilicon</term><term>Orgaontin</term><term>Pyrazole</term><term>Thiophene</term><term>X-ray</term></keywords><keywords scheme="Teeft" xml:lang="en"><term>Anal</term><term>Anion formation</term><term>Asymmetric unit</term><term>Bond angles</term><term>Bond lengths</term><term>Bond polarities</term><term>Buli</term><term>Calc</term><term>Chem</term><term>Chemical shifts</term><term>Colourless</term><term>Computer program</term><term>Crystal structure</term><term>Derivative</term><term>Diethyl</term><term>Diethyl ether</term><term>Elsevier science</term><term>Ether</term><term>Hexane</term><term>Lithiation</term><term>Mmol</term><term>Mossbauer</term><term>Organomet</term><term>Perkin trans</term><term>Petroleum ether</term><term>Phenyl groups</term><term>Phenyl rings</term><term>Polyhedron</term><term>Previous work</term><term>Pyrazole</term><term>Room temperature</term><term>Subsequent substitution</term><term>Tetrahedral geometry</term><term>Tributyltin chloride</term><term>Trimethylsilyl chloride</term><term>Trimethyltin chloride</term><term>Triphenyltin chloride</term><term>Unresolved</term><term>Vacuo</term><term>Vacuo removal</term><term>Vacuum distillation</term><term>White suspension</term><term>Yellow solution</term><term>Yellow suspension</term></keywords></textClass><langUsage><language ident="en">en</language></langUsage></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Abstract: C-organostannyl- and organosilyl-derivatives of 2-(thien-2-ylmethyl)thiophene and 1-[(1H-pyrazol-1-yl)methyl]-1H-pyrazole have been synthesised and characterised spectroscopically. Lithiation and subsequent substitution by R3M takes place at the 5,5′ positions for both bis-heterocycles, and this is confirmed by the X-ray structure of 1,1′-[5,5′-(Ph3Sn)C3N2]2CH2.</div><div type="abstract">C-organostannyl- and organosilyl-derivatives of 2-(thien-2-ylmethyl)thiophene and 1-[(1H-pyrazol-1-yl)methyl]-1H-pyrazole have been synthesised. Substitution by R3M takes place at the 5,5′ positions for both bis-heterocycles and this is confirmed by the X-ray structure of 1,1′-(5,5′-(Ph3Sn)C3N2]2CH2.loc1 </div></front></TEI><istex><corpusName>elsevier</corpusName><keywords><teeft><json:string>mmol</json:string><json:string>chem</json:string><json:string>anal</json:string><json:string>calc</json:string><json:string>diethyl</json:string><json:string>diethyl ether</json:string><json:string>colourless</json:string><json:string>hexane</json:string><json:string>buli</json:string><json:string>mossbauer</json:string><json:string>ether</json:string><json:string>room temperature</json:string><json:string>pyrazole</json:string><json:string>yellow solution</json:string><json:string>polyhedron</json:string><json:string>lithiation</json:string><json:string>vacuo</json:string><json:string>organomet</json:string><json:string>vacuo removal</json:string><json:string>bond lengths</json:string><json:string>bond angles</json:string><json:string>tetrahedral geometry</json:string><json:string>derivative</json:string><json:string>trimethylsilyl chloride</json:string><json:string>unresolved</json:string><json:string>petroleum ether</json:string><json:string>subsequent substitution</json:string><json:string>trimethyltin chloride</json:string><json:string>yellow suspension</json:string><json:string>phenyl rings</json:string><json:string>asymmetric unit</json:string><json:string>tributyltin chloride</json:string><json:string>elsevier science</json:string><json:string>anion formation</json:string><json:string>vacuum distillation</json:string><json:string>previous work</json:string><json:string>crystal structure</json:string><json:string>chemical shifts</json:string><json:string>bond polarities</json:string><json:string>phenyl groups</json:string><json:string>computer program</json:string><json:string>perkin trans</json:string><json:string>white suspension</json:string><json:string>triphenyltin chloride</json:string></teeft></keywords><author><json:item><name>Michael S. Hill</name><affiliations><json:string>Department of Chemistry, University of Bath, Claverton Down, Bath BA2 7AY, UK</json:string></affiliations></json:item><json:item><name>Mary F. Mahon</name><affiliations><json:string>Department of Chemistry, University of Bath, Claverton Down, Bath BA2 7AY, UK</json:string></affiliations></json:item><json:item><name>John M.G. McGinley</name><affiliations><json:string>Department of Chemistry, University of Bath, Claverton Down, Bath BA2 7AY, UK</json:string></affiliations></json:item><json:item><name>Kieran C. 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Lithiation and subsequent substitution by R3M takes place at the 5,5′ positions for both bis-heterocycles, and this is confirmed by the X-ray structure of 1,1′-[5,5′-(Ph3Sn)C3N2]2CH2.</abstract><qualityIndicators><score>7.37</score><pdfWordCount>4902</pdfWordCount><pdfCharCount>30322</pdfCharCount><pdfVersion>1.2</pdfVersion><pdfPageCount>8</pdfPageCount><pdfPageSize>552 x 752 pts</pdfPageSize><refBibsNative>true</refBibsNative><abstractWordCount>39</abstractWordCount><abstractCharCount>374</abstractCharCount><keywordCount>6</keywordCount></qualityIndicators><title>The synthesis and characterisation of C -triorganometallated (metal=Sn, Si) bis-(thienyl)- and bis-(pyrazolyl)alkanes, including the crystal structure of [(Ph3Sn)C3N2]2CH2</title><pii><json:string>S0277-5387(01)00799-9</json:string></pii><genre><json:string>research-article</json:string></genre><host><title>Polyhedron</title><language><json:string>unknown</json:string></language><publicationDate>2001</publicationDate><issn><json:string>0277-5387</json:string></issn><pii><json:string>S0277-5387(00)X0357-9</json:string></pii><volume>20</volume><issue>15–16</issue><pages><first>1995</first><last>2002</last></pages><genre><json:string>journal</json:string></genre></host><namedEntities><unitex><date><json:string>36S</json:string><json:string>2001</json:string><json:string>24S</json:string><json:string>60S</json:string></date><geogName></geogName><orgName><json:string>Elsevier Science Ltd.</json:string><json:string>UK Received</json:string></orgName><orgName_funder></orgName_funder><orgName_provider></orgName_provider><persName><json:string>Kieran C. 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Thermal ellipsoids are at the 30% probability level.</note><note type="content">Table 1: Crystallographic data for 10</note><note type="content">Table 2: Selected bond lengths (Å) and bond angles (°) for 10</note></notesStmt><sourceDesc><biblStruct type="inbook"><analytic><title level="a" type="main" xml:lang="en">The synthesis and characterisation of C -triorganometallated (metal=Sn, Si) bis-(thienyl)- and bis-(pyrazolyl)alkanes, including the crystal structure of [(Ph3Sn)C3N2]2CH2</title><author xml:id="author-0000"><persName><forename type="first">Michael S.</forename><surname>Hill</surname></persName><affiliation>Department of Chemistry, University of Bath, Claverton Down, Bath BA2 7AY, UK</affiliation></author><author xml:id="author-0001"><persName><forename type="first">Mary F.</forename><surname>Mahon</surname></persName><affiliation>Department of Chemistry, University of Bath, Claverton Down, Bath BA2 7AY, UK</affiliation></author><author xml:id="author-0002"><persName><forename type="first">John M.G.</forename><surname>McGinley</surname></persName><affiliation>Department of Chemistry, University of Bath, Claverton Down, Bath BA2 7AY, UK</affiliation></author><author xml:id="author-0003"><persName><forename type="first">Kieran C.</forename><surname>Molloy</surname></persName><email>chskcm@bath.ac.uk</email><note type="correspondence"><p>Corresponding author. Tel.: +44-1225-826382; fax: +44-1225-826231</p></note><affiliation>Department of Chemistry, University of Bath, Claverton Down, Bath BA2 7AY, UK</affiliation></author><idno type="istex">2C9D4E77B75296C010C26C236FE17F62B7ABA8EC</idno><idno type="ark">ark:/67375/6H6-4JK9MTBJ-T</idno><idno type="DOI">10.1016/S0277-5387(01)00799-9</idno><idno type="PII">S0277-5387(01)00799-9</idno></analytic><monogr><title level="j">Polyhedron</title><title level="j" type="abbrev">POLY</title><idno type="pISSN">0277-5387</idno><idno type="PII">S0277-5387(00)X0357-9</idno><imprint><publisher>ELSEVIER</publisher><date type="published" when="2001"></date><biblScope unit="volume">20</biblScope><biblScope unit="issue">15–16</biblScope><biblScope unit="page" from="1995">1995</biblScope><biblScope unit="page" to="2002">2002</biblScope></imprint></monogr></biblStruct></sourceDesc></fileDesc><profileDesc><creation><date>2001</date></creation><langUsage><language ident="en">en</language></langUsage><abstract xml:lang="en"><p>Abstract: C-organostannyl- and organosilyl-derivatives of 2-(thien-2-ylmethyl)thiophene and 1-[(1H-pyrazol-1-yl)methyl]-1H-pyrazole have been synthesised and characterised spectroscopically. Lithiation and subsequent substitution by R3M takes place at the 5,5′ positions for both bis-heterocycles, and this is confirmed by the X-ray structure of 1,1′-[5,5′-(Ph3Sn)C3N2]2CH2.</p></abstract><abstract style="graphical"><p>C-organostannyl- and organosilyl-derivatives of 2-(thien-2-ylmethyl)thiophene and 1-[(1H-pyrazol-1-yl)methyl]-1H-pyrazole have been synthesised. Substitution by R3M takes place at the 5,5′ positions for both bis-heterocycles and this is confirmed by the X-ray structure of 1,1′-(5,5′-(Ph3Sn)C3N2]2CH2.loc1</p></abstract><textClass xml:lang="en"><keywords scheme="keyword"><list><head>Keywords</head><item><term>Orgaontin</term></item><item><term>Organosilicon</term></item><item><term>Thiophene</term></item><item><term>Pyrazole</term></item><item><term>X-ray</term></item><item><term>Mössbauer</term></item></list></keywords></textClass></profileDesc><revisionDesc><change when="2001">Published</change></revisionDesc></teiHeader></istex:fulltextTEI><json:item><extension>txt</extension><original>false</original><mimetype>text/plain</mimetype><uri>https://api.istex.fr/ark:/67375/6H6-4JK9MTBJ-T/fulltext.txt</uri></json:item></fulltext><metadata><istex:metadataXml wicri:clean="Elsevier, elements deleted: ce:floats; body; tail"><istex:xmlDeclaration>version="1.0" encoding="utf-8"</istex:xmlDeclaration><istex:docType PUBLIC="-//ES//DTD journal article DTD version 4.5.2//EN//XML" URI="art452.dtd" name="istex:docType"><istex:entity SYSTEM="loc1" NDATA="IMAGE" name="loc1"></istex:entity><istex:entity SYSTEM="fx1" NDATA="IMAGE" name="fx1"></istex:entity><istex:entity SYSTEM="gr1" NDATA="IMAGE" name="gr1"></istex:entity><istex:entity SYSTEM="fx2" NDATA="IMAGE" name="fx2"></istex:entity><istex:entity SYSTEM="fx3" NDATA="IMAGE" name="fx3"></istex:entity></istex:docType><istex:document><converted-article version="4.5.2" docsubtype="fla" xml:lang="en"><item-info><jid>POLY</jid><aid>3943</aid><ce:pii>S0277-5387(01)00799-9</ce:pii><ce:doi>10.1016/S0277-5387(01)00799-9</ce:doi><ce:copyright type="full-transfer" year="2001">Elsevier Science Ltd</ce:copyright></item-info><head><ce:title>The synthesis and characterisation of <ce:italic>C</ce:italic>-triorganometallated (metal=Sn, Si) bis-(thienyl)- and bis-(pyrazolyl)alkanes, including the crystal structure of [(Ph<ce:inf>3</ce:inf>Sn)C<ce:inf>3</ce:inf>N<ce:inf>2</ce:inf>]<ce:inf>2</ce:inf>CH<ce:inf>2</ce:inf></ce:title><ce:author-group><ce:author><ce:given-name>Michael S.</ce:given-name><ce:surname>Hill</ce:surname></ce:author><ce:author><ce:given-name>Mary F.</ce:given-name><ce:surname>Mahon</ce:surname></ce:author><ce:author><ce:given-name>John M.G.</ce:given-name><ce:surname>McGinley</ce:surname></ce:author><ce:author><ce:given-name>Kieran C.</ce:given-name><ce:surname>Molloy</ce:surname><ce:cross-ref refid="COR1">*</ce:cross-ref><ce:e-address type="email">chskcm@bath.ac.uk</ce:e-address></ce:author><ce:affiliation><ce:textfn>Department of Chemistry, University of Bath, Claverton Down, Bath BA2 7AY, UK</ce:textfn></ce:affiliation><ce:correspondence id="COR1"><ce:label>*</ce:label><ce:text>Corresponding author. Tel.: +44-1225-826382; fax: +44-1225-826231</ce:text></ce:correspondence></ce:author-group><ce:date-received day="19" month="1" year="2001"></ce:date-received><ce:date-accepted day="26" month="3" year="2001"></ce:date-accepted><ce:abstract><ce:section-title>Abstract</ce:section-title><ce:abstract-sec><ce:simple-para><ce:italic>C</ce:italic>-organostannyl- and organosilyl-derivatives of 2-(thien-2-ylmethyl)thiophene and 1-[(1<ce:italic>H</ce:italic>-pyrazol-1-yl)methyl]-1<ce:italic>H</ce:italic>-pyrazole have been synthesised and characterised spectroscopically. Lithiation and subsequent substitution by R<ce:inf>3</ce:inf>M takes place at the 5,5′ positions for both bis-heterocycles, and this is confirmed by the X-ray structure of 1,1′-[5,5′-(Ph<ce:inf>3</ce:inf>Sn)C<ce:inf>3</ce:inf>N<ce:inf>2</ce:inf>]<ce:inf>2</ce:inf>CH<ce:inf>2</ce:inf>.</ce:simple-para></ce:abstract-sec></ce:abstract><ce:abstract class="graphical"><ce:abstract-sec><ce:simple-para><ce:italic>C</ce:italic>-organostannyl- and organosilyl-derivatives of 2-(thien-2-ylmethyl)thiophene and 1-[(1<ce:italic>H</ce:italic>-pyrazol-1-yl)methyl]-1<ce:italic>H</ce:italic>-pyrazole have been synthesised. Substitution by R<ce:inf>3</ce:inf>M takes place at the 5,5′ positions for both bis-heterocycles and this is confirmed by the X-ray structure of 1,1′-(5,5′-(Ph<ce:inf>3</ce:inf>Sn)C<ce:inf>3</ce:inf>N<ce:inf>2</ce:inf>]<ce:inf>2</ce:inf>CH<ce:inf>2</ce:inf>.</ce:simple-para></ce:abstract-sec><ce:figure><ce:link locator="loc1"></ce:link></ce:figure></ce:abstract><ce:keywords class="keyword"><ce:section-title>Keywords</ce:section-title><ce:keyword><ce:text>Orgaontin</ce:text></ce:keyword><ce:keyword><ce:text>Organosilicon</ce:text></ce:keyword><ce:keyword><ce:text>Thiophene</ce:text></ce:keyword><ce:keyword><ce:text>Pyrazole</ce:text></ce:keyword><ce:keyword><ce:text>X-ray</ce:text></ce:keyword><ce:keyword><ce:text>Mössbauer</ce:text></ce:keyword></ce:keywords></head></converted-article></istex:document></istex:metadataXml><mods version="3.6"><titleInfo lang="en"><title>The synthesis and characterisation of C -triorganometallated (metal=Sn, Si) bis-(thienyl)- and bis-(pyrazolyl)alkanes, including the crystal structure of [(Ph3Sn)C3N2]2CH2</title></titleInfo><titleInfo type="alternative" lang="en" contentType="CDATA"><title>The synthesis and characterisation of</title></titleInfo><name type="personal"><namePart type="given">Michael S.</namePart><namePart type="family">Hill</namePart><affiliation>Department of Chemistry, University of Bath, Claverton Down, Bath BA2 7AY, UK</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Mary F.</namePart><namePart type="family">Mahon</namePart><affiliation>Department of Chemistry, University of Bath, Claverton Down, Bath BA2 7AY, UK</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">John M.G.</namePart><namePart type="family">McGinley</namePart><affiliation>Department of Chemistry, University of Bath, Claverton Down, Bath BA2 7AY, UK</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Kieran C.</namePart><namePart type="family">Molloy</namePart><affiliation>Department of Chemistry, University of Bath, Claverton Down, Bath BA2 7AY, UK</affiliation><affiliation>E-mail: chskcm@bath.ac.uk</affiliation><description>Corresponding author. Tel.: +44-1225-826382; fax: +44-1225-826231</description><role><roleTerm type="text">author</roleTerm></role></name><typeOfResource>text</typeOfResource><genre type="research-article" displayLabel="Full-length article" authority="ISTEX" authorityURI="https://content-type.data.istex.fr" valueURI="https://content-type.data.istex.fr/ark:/67375/XTP-1JC4F85T-7">research-article</genre><originInfo><publisher>ELSEVIER</publisher><dateIssued encoding="w3cdtf">2001</dateIssued><copyrightDate encoding="w3cdtf">2001</copyrightDate></originInfo><language><languageTerm type="code" authority="iso639-2b">eng</languageTerm><languageTerm type="code" authority="rfc3066">en</languageTerm></language><abstract lang="en">Abstract: C-organostannyl- and organosilyl-derivatives of 2-(thien-2-ylmethyl)thiophene and 1-[(1H-pyrazol-1-yl)methyl]-1H-pyrazole have been synthesised and characterised spectroscopically. Lithiation and subsequent substitution by R3M takes place at the 5,5′ positions for both bis-heterocycles, and this is confirmed by the X-ray structure of 1,1′-[5,5′-(Ph3Sn)C3N2]2CH2.</abstract><abstract type="graphical">C-organostannyl- and organosilyl-derivatives of 2-(thien-2-ylmethyl)thiophene and 1-[(1H-pyrazol-1-yl)methyl]-1H-pyrazole have been synthesised. Substitution by R3M takes place at the 5,5′ positions for both bis-heterocycles and this is confirmed by the X-ray structure of 1,1′-(5,5′-(Ph3Sn)C3N2]2CH2.loc1 </abstract><note type="content">Fig. 1: The asymmetric unit of 10 showing the labelling scheme used in the text. Thermal ellipsoids are at the 30% probability level.</note><note type="content">Table 1: Crystallographic data for 10</note><note type="content">Table 2: Selected bond lengths (Å) and bond angles (°) for 10</note><subject lang="en"><genre>Keywords</genre><topic>Orgaontin</topic><topic>Organosilicon</topic><topic>Thiophene</topic><topic>Pyrazole</topic><topic>X-ray</topic><topic>Mössbauer</topic></subject><relatedItem type="host"><titleInfo><title>Polyhedron</title></titleInfo><titleInfo type="abbreviated"><title>POLY</title></titleInfo><genre type="journal" authority="ISTEX" authorityURI="https://publication-type.data.istex.fr" valueURI="https://publication-type.data.istex.fr/ark:/67375/JMC-0GLKJH51-B">journal</genre><originInfo><publisher>ELSEVIER</publisher><dateIssued encoding="w3cdtf">2001</dateIssued></originInfo><identifier type="ISSN">0277-5387</identifier><identifier type="PII">S0277-5387(00)X0357-9</identifier><part><date>2001</date><detail type="volume"><number>20</number><caption>vol.</caption></detail><detail type="issue"><number>15–16</number><caption>no.</caption></detail><extent unit="issue-pages"><start>1785</start><end>2093</end></extent><extent unit="pages"><start>1995</start><end>2002</end></extent></part></relatedItem><identifier type="istex">2C9D4E77B75296C010C26C236FE17F62B7ABA8EC</identifier><identifier type="ark">ark:/67375/6H6-4JK9MTBJ-T</identifier><identifier type="DOI">10.1016/S0277-5387(01)00799-9</identifier><identifier type="PII">S0277-5387(01)00799-9</identifier><accessCondition type="use and reproduction" contentType="copyright">©2001 Elsevier Science Ltd</accessCondition><recordInfo><recordContentSource authority="ISTEX" authorityURI="https://loaded-corpus.data.istex.fr" valueURI="https://loaded-corpus.data.istex.fr/ark:/67375/XBH-HKKZVM7B-M">elsevier</recordContentSource><recordOrigin>Elsevier Science Ltd, ©2001</recordOrigin></recordInfo></mods><json:item><extension>json</extension><original>false</original><mimetype>application/json</mimetype><uri>https://api.istex.fr/ark:/67375/6H6-4JK9MTBJ-T/record.json</uri></json:item></metadata><serie></serie></istex></record>Pour manipuler ce document sous Unix (Dilib)
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