Design and Development of Isocyanatoacrylates as Dental Adhesives
During the last 12 years, significant progress has been made in the development of dental adhesive systems. Some of the more promising systems are based on multifunctional structures that contain polymerizable vinyl double bonds and reactive isocyanate groups. The utility of compounds with such stru...
Gespeichert in:
Veröffentlicht in: | Journal of dental research 1996-02, Vol.75 (2), p.761-767 |
---|---|
Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 767 |
---|---|
container_issue | 2 |
container_start_page | 761 |
container_title | Journal of dental research |
container_volume | 75 |
creator | Chappelow, C.C. Byerley, T.J. Pinzino, C.S. Millich, F. Eick, J.D. |
description | During the last 12 years, significant progress has been made in the development of dental adhesive systems. Some of the more promising systems are based on multifunctional structures that contain polymerizable vinyl double bonds and reactive isocyanate groups. The utility of compounds with such structures as adhesives arises in part because their isocyanate functionality is available for reaction independently, without compromising the reactivity of the vinyl groups. The hypotheses tested in this investigation were: (1) that the monomer reactivity ratios (r1, r2) for the free-radical-initiated copolymerization of ethyl a-isocyanatoacrylate (a-EIA) and 2-isocyanatoethyl methacrylate (IEM) with selected vinyl monomers can be determined; (2) that these reactivity ratios can be used to establish Q (reactivity) and e (polarity) values for a-EIA and IEM; and (3) that these reactivity parameters can be useful in designing copolymers with controlled compositions for dental adhesive applications. The free-radical copolymerization characteristics of a-EIA and IEM were studied. The isocyanate monomers were copolymerized at seven comonomer ratios with n-butyl acrylate (NBA), methyl methacrylate (MMA), and styrene (STY). Reactivity ratios, r1 and r2, were calculated for each of the copolymer systems, giving: IEM (r1) = 0.38 and STY (r2) = 0.44; IEM (r1) = 1.19 and MMA (r2) = 0.84; IEM (r1) = 2.50 and NBA (r2) = 0.40; a-EIA (r1) = 2.20 and STY (r2) = 0.06; α-EIA (r1) = 7.00 and MMA (r2) = 0.10; and a-EIA (r1) = 23.50 and NBA (r2) = 0.04. The Q (reactivity) and e (polarity) values for IEM and a-EIA were calculated from r1 and r2 with use of the Alfrey-Price equations, giving, for IEM, Q = 0.89 and e = 0.60, and, for a-EIA, Q = 7.64 and e = 0.74. These reactivity parameters are useful for tailoring copolymers with controlled compositions and properties. Based on these calculated reactivity parameters, several copolymers of IEM [for example, IEM/2-hydroxyethyl methacrylate (HEMA)] are currently being prepared and evaluated as adhesives. |
doi_str_mv | 10.1177/00220345960750020501 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_78081036</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sage_id>10.1177_00220345960750020501</sage_id><sourcerecordid>78081036</sourcerecordid><originalsourceid>FETCH-LOGICAL-c467t-24862067e1458878e059ad94415fb9a66dcdd7fea0527474b159d0aca39481863</originalsourceid><addsrcrecordid>eNp9kE9Lw0AQxRdRaq1-A4WA4C06u9nNbo6l9U-h4EXPYZqd1JY0W7NJod_eDS0KIp6GYX7vzeMxds3hnnOtHwCEgESqLAWtwgIK-AkbciVlDCrjp2zYI3HPnLML79cAPBMmGbCBSZXSWgzZeEp-tawjrG00pR1Vbruhuo1cGc28K_ZYY-uwaPYVtuQj9IGqW6yisf0Iyh35S3ZWYuXp6jhH7P3p8W3yEs9fn2eT8TwuZKrbWEiTCkg1camM0YZCRLSZlFyViwzT1BbW6pIQlNBSywVXmQUsMMmk4SZNRuzu4Ltt3GdHvs03K19QVWFNrvO5NmA4JD14-wtcu66pQ7ZcJFyC0NokgZIHqmic9w2V-bZZbbDZ5xzyvt_8r36D7OZo3i02ZL9Fx0LDnR_uHpf08_hfzy-rH4CR</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2314027783</pqid></control><display><type>article</type><title>Design and Development of Isocyanatoacrylates as Dental Adhesives</title><source>Access via SAGE</source><source>MEDLINE</source><creator>Chappelow, C.C. ; Byerley, T.J. ; Pinzino, C.S. ; Millich, F. ; Eick, J.D.</creator><creatorcontrib>Chappelow, C.C. ; Byerley, T.J. ; Pinzino, C.S. ; Millich, F. ; Eick, J.D.</creatorcontrib><description>During the last 12 years, significant progress has been made in the development of dental adhesive systems. Some of the more promising systems are based on multifunctional structures that contain polymerizable vinyl double bonds and reactive isocyanate groups. The utility of compounds with such structures as adhesives arises in part because their isocyanate functionality is available for reaction independently, without compromising the reactivity of the vinyl groups. The hypotheses tested in this investigation were: (1) that the monomer reactivity ratios (r1, r2) for the free-radical-initiated copolymerization of ethyl a-isocyanatoacrylate (a-EIA) and 2-isocyanatoethyl methacrylate (IEM) with selected vinyl monomers can be determined; (2) that these reactivity ratios can be used to establish Q (reactivity) and e (polarity) values for a-EIA and IEM; and (3) that these reactivity parameters can be useful in designing copolymers with controlled compositions for dental adhesive applications. The free-radical copolymerization characteristics of a-EIA and IEM were studied. The isocyanate monomers were copolymerized at seven comonomer ratios with n-butyl acrylate (NBA), methyl methacrylate (MMA), and styrene (STY). Reactivity ratios, r1 and r2, were calculated for each of the copolymer systems, giving: IEM (r1) = 0.38 and STY (r2) = 0.44; IEM (r1) = 1.19 and MMA (r2) = 0.84; IEM (r1) = 2.50 and NBA (r2) = 0.40; a-EIA (r1) = 2.20 and STY (r2) = 0.06; α-EIA (r1) = 7.00 and MMA (r2) = 0.10; and a-EIA (r1) = 23.50 and NBA (r2) = 0.04. The Q (reactivity) and e (polarity) values for IEM and a-EIA were calculated from r1 and r2 with use of the Alfrey-Price equations, giving, for IEM, Q = 0.89 and e = 0.60, and, for a-EIA, Q = 7.64 and e = 0.74. These reactivity parameters are useful for tailoring copolymers with controlled compositions and properties. Based on these calculated reactivity parameters, several copolymers of IEM [for example, IEM/2-hydroxyethyl methacrylate (HEMA)] are currently being prepared and evaluated as adhesives.</description><identifier>ISSN: 0022-0345</identifier><identifier>EISSN: 1544-0591</identifier><identifier>DOI: 10.1177/00220345960750020501</identifier><identifier>PMID: 8655772</identifier><language>eng</language><publisher>Los Angeles, CA: SAGE Publications</publisher><subject>Acrylates - chemistry ; Acrylics ; Adhesives ; Adhesives - chemistry ; Calorimetry, Differential Scanning ; Chemical industry ; Chemical Phenomena ; Chemistry, Physical ; Copolymers ; Cyanoacrylates - chemistry ; Dental Materials - chemistry ; Dentistry ; Drug Design ; Free radicals ; Free Radicals - chemistry ; Isocyanates ; Isocyanates - chemistry ; Methacrylates - chemistry ; Methylmethacrylate ; Methylmethacrylates - chemistry ; Monomers ; Polarity ; Polymers - chemistry ; Spectroscopy, Fourier Transform Infrared ; Styrene ; Styrenes - chemistry ; Thermography ; Vinyl Compounds - chemistry</subject><ispartof>Journal of dental research, 1996-02, Vol.75 (2), p.761-767</ispartof><rights>19960201.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c467t-24862067e1458878e059ad94415fb9a66dcdd7fea0527474b159d0aca39481863</citedby><cites>FETCH-LOGICAL-c467t-24862067e1458878e059ad94415fb9a66dcdd7fea0527474b159d0aca39481863</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.sagepub.com/doi/pdf/10.1177/00220345960750020501$$EPDF$$P50$$Gsage$$H</linktopdf><linktohtml>$$Uhttps://journals.sagepub.com/doi/10.1177/00220345960750020501$$EHTML$$P50$$Gsage$$H</linktohtml><link.rule.ids>314,780,784,21819,27924,27925,43621,43622</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8655772$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chappelow, C.C.</creatorcontrib><creatorcontrib>Byerley, T.J.</creatorcontrib><creatorcontrib>Pinzino, C.S.</creatorcontrib><creatorcontrib>Millich, F.</creatorcontrib><creatorcontrib>Eick, J.D.</creatorcontrib><title>Design and Development of Isocyanatoacrylates as Dental Adhesives</title><title>Journal of dental research</title><addtitle>J Dent Res</addtitle><description>During the last 12 years, significant progress has been made in the development of dental adhesive systems. Some of the more promising systems are based on multifunctional structures that contain polymerizable vinyl double bonds and reactive isocyanate groups. The utility of compounds with such structures as adhesives arises in part because their isocyanate functionality is available for reaction independently, without compromising the reactivity of the vinyl groups. The hypotheses tested in this investigation were: (1) that the monomer reactivity ratios (r1, r2) for the free-radical-initiated copolymerization of ethyl a-isocyanatoacrylate (a-EIA) and 2-isocyanatoethyl methacrylate (IEM) with selected vinyl monomers can be determined; (2) that these reactivity ratios can be used to establish Q (reactivity) and e (polarity) values for a-EIA and IEM; and (3) that these reactivity parameters can be useful in designing copolymers with controlled compositions for dental adhesive applications. The free-radical copolymerization characteristics of a-EIA and IEM were studied. The isocyanate monomers were copolymerized at seven comonomer ratios with n-butyl acrylate (NBA), methyl methacrylate (MMA), and styrene (STY). Reactivity ratios, r1 and r2, were calculated for each of the copolymer systems, giving: IEM (r1) = 0.38 and STY (r2) = 0.44; IEM (r1) = 1.19 and MMA (r2) = 0.84; IEM (r1) = 2.50 and NBA (r2) = 0.40; a-EIA (r1) = 2.20 and STY (r2) = 0.06; α-EIA (r1) = 7.00 and MMA (r2) = 0.10; and a-EIA (r1) = 23.50 and NBA (r2) = 0.04. The Q (reactivity) and e (polarity) values for IEM and a-EIA were calculated from r1 and r2 with use of the Alfrey-Price equations, giving, for IEM, Q = 0.89 and e = 0.60, and, for a-EIA, Q = 7.64 and e = 0.74. These reactivity parameters are useful for tailoring copolymers with controlled compositions and properties. Based on these calculated reactivity parameters, several copolymers of IEM [for example, IEM/2-hydroxyethyl methacrylate (HEMA)] are currently being prepared and evaluated as adhesives.</description><subject>Acrylates - chemistry</subject><subject>Acrylics</subject><subject>Adhesives</subject><subject>Adhesives - chemistry</subject><subject>Calorimetry, Differential Scanning</subject><subject>Chemical industry</subject><subject>Chemical Phenomena</subject><subject>Chemistry, Physical</subject><subject>Copolymers</subject><subject>Cyanoacrylates - chemistry</subject><subject>Dental Materials - chemistry</subject><subject>Dentistry</subject><subject>Drug Design</subject><subject>Free radicals</subject><subject>Free Radicals - chemistry</subject><subject>Isocyanates</subject><subject>Isocyanates - chemistry</subject><subject>Methacrylates - chemistry</subject><subject>Methylmethacrylate</subject><subject>Methylmethacrylates - chemistry</subject><subject>Monomers</subject><subject>Polarity</subject><subject>Polymers - chemistry</subject><subject>Spectroscopy, Fourier Transform Infrared</subject><subject>Styrene</subject><subject>Styrenes - chemistry</subject><subject>Thermography</subject><subject>Vinyl Compounds - chemistry</subject><issn>0022-0345</issn><issn>1544-0591</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1996</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp9kE9Lw0AQxRdRaq1-A4WA4C06u9nNbo6l9U-h4EXPYZqd1JY0W7NJod_eDS0KIp6GYX7vzeMxds3hnnOtHwCEgESqLAWtwgIK-AkbciVlDCrjp2zYI3HPnLML79cAPBMmGbCBSZXSWgzZeEp-tawjrG00pR1Vbruhuo1cGc28K_ZYY-uwaPYVtuQj9IGqW6yisf0Iyh35S3ZWYuXp6jhH7P3p8W3yEs9fn2eT8TwuZKrbWEiTCkg1camM0YZCRLSZlFyViwzT1BbW6pIQlNBSywVXmQUsMMmk4SZNRuzu4Ltt3GdHvs03K19QVWFNrvO5NmA4JD14-wtcu66pQ7ZcJFyC0NokgZIHqmic9w2V-bZZbbDZ5xzyvt_8r36D7OZo3i02ZL9Fx0LDnR_uHpf08_hfzy-rH4CR</recordid><startdate>19960201</startdate><enddate>19960201</enddate><creator>Chappelow, C.C.</creator><creator>Byerley, T.J.</creator><creator>Pinzino, C.S.</creator><creator>Millich, F.</creator><creator>Eick, J.D.</creator><general>SAGE Publications</general><general>SAGE PUBLICATIONS, INC</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RQ</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>S0X</scope><scope>U9A</scope><scope>7X8</scope></search><sort><creationdate>19960201</creationdate><title>Design and Development of Isocyanatoacrylates as Dental Adhesives</title><author>Chappelow, C.C. ; Byerley, T.J. ; Pinzino, C.S. ; Millich, F. ; Eick, J.D.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c467t-24862067e1458878e059ad94415fb9a66dcdd7fea0527474b159d0aca39481863</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1996</creationdate><topic>Acrylates - chemistry</topic><topic>Acrylics</topic><topic>Adhesives</topic><topic>Adhesives - chemistry</topic><topic>Calorimetry, Differential Scanning</topic><topic>Chemical industry</topic><topic>Chemical Phenomena</topic><topic>Chemistry, Physical</topic><topic>Copolymers</topic><topic>Cyanoacrylates - chemistry</topic><topic>Dental Materials - chemistry</topic><topic>Dentistry</topic><topic>Drug Design</topic><topic>Free radicals</topic><topic>Free Radicals - chemistry</topic><topic>Isocyanates</topic><topic>Isocyanates - chemistry</topic><topic>Methacrylates - chemistry</topic><topic>Methylmethacrylate</topic><topic>Methylmethacrylates - chemistry</topic><topic>Monomers</topic><topic>Polarity</topic><topic>Polymers - chemistry</topic><topic>Spectroscopy, Fourier Transform Infrared</topic><topic>Styrene</topic><topic>Styrenes - chemistry</topic><topic>Thermography</topic><topic>Vinyl Compounds - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chappelow, C.C.</creatorcontrib><creatorcontrib>Byerley, T.J.</creatorcontrib><creatorcontrib>Pinzino, C.S.</creatorcontrib><creatorcontrib>Millich, F.</creatorcontrib><creatorcontrib>Eick, J.D.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Career & Technical Education Database</collection><collection>Nursing & Allied Health Database</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>SIRS Editorial</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of dental research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chappelow, C.C.</au><au>Byerley, T.J.</au><au>Pinzino, C.S.</au><au>Millich, F.</au><au>Eick, J.D.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Design and Development of Isocyanatoacrylates as Dental Adhesives</atitle><jtitle>Journal of dental research</jtitle><addtitle>J Dent Res</addtitle><date>1996-02-01</date><risdate>1996</risdate><volume>75</volume><issue>2</issue><spage>761</spage><epage>767</epage><pages>761-767</pages><issn>0022-0345</issn><eissn>1544-0591</eissn><abstract>During the last 12 years, significant progress has been made in the development of dental adhesive systems. Some of the more promising systems are based on multifunctional structures that contain polymerizable vinyl double bonds and reactive isocyanate groups. The utility of compounds with such structures as adhesives arises in part because their isocyanate functionality is available for reaction independently, without compromising the reactivity of the vinyl groups. The hypotheses tested in this investigation were: (1) that the monomer reactivity ratios (r1, r2) for the free-radical-initiated copolymerization of ethyl a-isocyanatoacrylate (a-EIA) and 2-isocyanatoethyl methacrylate (IEM) with selected vinyl monomers can be determined; (2) that these reactivity ratios can be used to establish Q (reactivity) and e (polarity) values for a-EIA and IEM; and (3) that these reactivity parameters can be useful in designing copolymers with controlled compositions for dental adhesive applications. The free-radical copolymerization characteristics of a-EIA and IEM were studied. The isocyanate monomers were copolymerized at seven comonomer ratios with n-butyl acrylate (NBA), methyl methacrylate (MMA), and styrene (STY). Reactivity ratios, r1 and r2, were calculated for each of the copolymer systems, giving: IEM (r1) = 0.38 and STY (r2) = 0.44; IEM (r1) = 1.19 and MMA (r2) = 0.84; IEM (r1) = 2.50 and NBA (r2) = 0.40; a-EIA (r1) = 2.20 and STY (r2) = 0.06; α-EIA (r1) = 7.00 and MMA (r2) = 0.10; and a-EIA (r1) = 23.50 and NBA (r2) = 0.04. The Q (reactivity) and e (polarity) values for IEM and a-EIA were calculated from r1 and r2 with use of the Alfrey-Price equations, giving, for IEM, Q = 0.89 and e = 0.60, and, for a-EIA, Q = 7.64 and e = 0.74. These reactivity parameters are useful for tailoring copolymers with controlled compositions and properties. Based on these calculated reactivity parameters, several copolymers of IEM [for example, IEM/2-hydroxyethyl methacrylate (HEMA)] are currently being prepared and evaluated as adhesives.</abstract><cop>Los Angeles, CA</cop><pub>SAGE Publications</pub><pmid>8655772</pmid><doi>10.1177/00220345960750020501</doi><tpages>7</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0022-0345 |
ispartof | Journal of dental research, 1996-02, Vol.75 (2), p.761-767 |
issn | 0022-0345 1544-0591 |
language | eng |
recordid | cdi_proquest_miscellaneous_78081036 |
source | Access via SAGE; MEDLINE |
subjects | Acrylates - chemistry Acrylics Adhesives Adhesives - chemistry Calorimetry, Differential Scanning Chemical industry Chemical Phenomena Chemistry, Physical Copolymers Cyanoacrylates - chemistry Dental Materials - chemistry Dentistry Drug Design Free radicals Free Radicals - chemistry Isocyanates Isocyanates - chemistry Methacrylates - chemistry Methylmethacrylate Methylmethacrylates - chemistry Monomers Polarity Polymers - chemistry Spectroscopy, Fourier Transform Infrared Styrene Styrenes - chemistry Thermography Vinyl Compounds - chemistry |
title | Design and Development of Isocyanatoacrylates as Dental Adhesives |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-30T20%3A42%3A57IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Design%20and%20Development%20of%20Isocyanatoacrylates%20as%20Dental%20Adhesives&rft.jtitle=Journal%20of%20dental%20research&rft.au=Chappelow,%20C.C.&rft.date=1996-02-01&rft.volume=75&rft.issue=2&rft.spage=761&rft.epage=767&rft.pages=761-767&rft.issn=0022-0345&rft.eissn=1544-0591&rft_id=info:doi/10.1177/00220345960750020501&rft_dat=%3Cproquest_cross%3E78081036%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2314027783&rft_id=info:pmid/8655772&rft_sage_id=10.1177_00220345960750020501&rfr_iscdi=true |