Study of fluoroalkylsilanes, a new class of amphiphilic oligomers: Determination of end groups and chain length
Radiation-initiated polymerization of tetrafluoroethylene (TFE) in the liquid alkylsilanes Si(CH 3 ) 4 (I), C 2 H 5 Si(CH 3 ) 3 (II), and ClSi(CH 3 ) 3 (III) produces fluoroalkylsilane oligomers with the general formula R(C 2 F 4 ) n X, where X = H or Cl in I, II, and III and R is one of the radical...
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creator | Kim, I. P. Benderskii, V. A. Martynenko, V. M. Chernyak, A. V. |
description | Radiation-initiated polymerization of tetrafluoroethylene (TFE) in the liquid alkylsilanes Si(CH
3
)
4
(I), C
2
H
5
Si(CH
3
)
3
(II), and ClSi(CH
3
)
3
(III) produces fluoroalkylsilane oligomers with the general formula R(C
2
F
4
)
n
X, where X = H or Cl in I, II, and III and R is one of the radicals generated by the abstraction of H from the methyl and ethyl groups in I and II or Cl detachment from III. The nature of R has been determined using an NMR technique, and the molecular mass distribution (MMD) has been found from abundances in anion progressions in mass spectra and from DTG and GPC data. At initial TFE concentrations (
C
0
) changed from 0.4, 1, and 0.13 to 1, 2.7, and 0.7 mol/L in I, II and III, respectively, the average chain length 〈
n
〉 increases from 4–5 to 10–12 and the MMD changes from the unimodal to the bimodal pattern in which the proportion of oligomers with
n
< 6 decreases with increasing
C
0
. As 〈
n
〉 increases and the MMD changes, the homogeneous solution becomes colloidal and then turns into a gel. The colloidal particles are largely composed of long oligomers, and the number of solvent molecules per C
2
F
4
unit decreases with an increase in
C
0
and is 4–7 in the gel. |
doi_str_mv | 10.1134/S0018143917040063 |
format | Article |
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3
)
4
(I), C
2
H
5
Si(CH
3
)
3
(II), and ClSi(CH
3
)
3
(III) produces fluoroalkylsilane oligomers with the general formula R(C
2
F
4
)
n
X, where X = H or Cl in I, II, and III and R is one of the radicals generated by the abstraction of H from the methyl and ethyl groups in I and II or Cl detachment from III. The nature of R has been determined using an NMR technique, and the molecular mass distribution (MMD) has been found from abundances in anion progressions in mass spectra and from DTG and GPC data. At initial TFE concentrations (
C
0
) changed from 0.4, 1, and 0.13 to 1, 2.7, and 0.7 mol/L in I, II and III, respectively, the average chain length 〈
n
〉 increases from 4–5 to 10–12 and the MMD changes from the unimodal to the bimodal pattern in which the proportion of oligomers with
n
< 6 decreases with increasing
C
0
. As 〈
n
〉 increases and the MMD changes, the homogeneous solution becomes colloidal and then turns into a gel. The colloidal particles are largely composed of long oligomers, and the number of solvent molecules per C
2
F
4
unit decreases with an increase in
C
0
and is 4–7 in the gel.</description><identifier>ISSN: 0018-1439</identifier><identifier>EISSN: 1608-3148</identifier><identifier>DOI: 10.1134/S0018143917040063</identifier><language>eng</language><publisher>Moscow: Pleiades Publishing</publisher><subject>Chains (polymeric) ; Chemistry ; Chemistry and Materials Science ; Colloids ; Mass distribution ; Mass spectra ; Mass spectroscopy ; Nanostructured Systems and Materials ; NMR ; Nuclear magnetic resonance ; Oligomers ; Physical Chemistry ; Polymerization ; Progressions</subject><ispartof>High energy chemistry, 2017-07, Vol.51 (4), p.277-284</ispartof><rights>Pleiades Publishing, Ltd. 2017</rights><rights>Copyright Springer Science & Business Media 2017</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c316t-d6adddba2530596e0affd119aa37bcf764411b1c7d1d9dff98e12f42df9628ef3</citedby><cites>FETCH-LOGICAL-c316t-d6adddba2530596e0affd119aa37bcf764411b1c7d1d9dff98e12f42df9628ef3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1134/S0018143917040063$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1134/S0018143917040063$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids></links><search><creatorcontrib>Kim, I. P.</creatorcontrib><creatorcontrib>Benderskii, V. A.</creatorcontrib><creatorcontrib>Martynenko, V. M.</creatorcontrib><creatorcontrib>Chernyak, A. V.</creatorcontrib><title>Study of fluoroalkylsilanes, a new class of amphiphilic oligomers: Determination of end groups and chain length</title><title>High energy chemistry</title><addtitle>High Energy Chem</addtitle><description>Radiation-initiated polymerization of tetrafluoroethylene (TFE) in the liquid alkylsilanes Si(CH
3
)
4
(I), C
2
H
5
Si(CH
3
)
3
(II), and ClSi(CH
3
)
3
(III) produces fluoroalkylsilane oligomers with the general formula R(C
2
F
4
)
n
X, where X = H or Cl in I, II, and III and R is one of the radicals generated by the abstraction of H from the methyl and ethyl groups in I and II or Cl detachment from III. The nature of R has been determined using an NMR technique, and the molecular mass distribution (MMD) has been found from abundances in anion progressions in mass spectra and from DTG and GPC data. At initial TFE concentrations (
C
0
) changed from 0.4, 1, and 0.13 to 1, 2.7, and 0.7 mol/L in I, II and III, respectively, the average chain length 〈
n
〉 increases from 4–5 to 10–12 and the MMD changes from the unimodal to the bimodal pattern in which the proportion of oligomers with
n
< 6 decreases with increasing
C
0
. As 〈
n
〉 increases and the MMD changes, the homogeneous solution becomes colloidal and then turns into a gel. The colloidal particles are largely composed of long oligomers, and the number of solvent molecules per C
2
F
4
unit decreases with an increase in
C
0
and is 4–7 in the gel.</description><subject>Chains (polymeric)</subject><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Colloids</subject><subject>Mass distribution</subject><subject>Mass spectra</subject><subject>Mass spectroscopy</subject><subject>Nanostructured Systems and Materials</subject><subject>NMR</subject><subject>Nuclear magnetic resonance</subject><subject>Oligomers</subject><subject>Physical Chemistry</subject><subject>Polymerization</subject><subject>Progressions</subject><issn>0018-1439</issn><issn>1608-3148</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNp1kE9LxDAQxYMouK5-AG8Br1Znmm7beBP_w4KH1XPJNkk3a5rUpEX229uyHgQRBmbg_d4beIScI1whsux6BYAlZoxjARlAzg7IDHMoE4ZZeUhmk5xM-jE5iXELAAtgMCN-1Q9yR72m2g4-eGE_djYaK5yKl1RQp75obUWMEyLabmPGsaam3prGtyrEG3qvehVa40RvvJs45SRtgh-6SMV41hthHLXKNf3mlBxpYaM6-9lz8v748Hb3nCxfn17ubpdJzTDvE5kLKeVapAsGC54rEFpLRC4EK9a1LvIsQ1xjXUiUXGrNS4WpzlKpeZ6WSrM5udjndsF_Dir21dYPwY0vK-RpihwZwkjhnqqDjzEoXXXBtCLsKoRq6rX60-voSfeeOLKuUeFX8r-mb2K2e5M</recordid><startdate>20170701</startdate><enddate>20170701</enddate><creator>Kim, I. P.</creator><creator>Benderskii, V. A.</creator><creator>Martynenko, V. M.</creator><creator>Chernyak, A. V.</creator><general>Pleiades Publishing</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20170701</creationdate><title>Study of fluoroalkylsilanes, a new class of amphiphilic oligomers: Determination of end groups and chain length</title><author>Kim, I. P. ; Benderskii, V. A. ; Martynenko, V. M. ; Chernyak, A. V.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c316t-d6adddba2530596e0affd119aa37bcf764411b1c7d1d9dff98e12f42df9628ef3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Chains (polymeric)</topic><topic>Chemistry</topic><topic>Chemistry and Materials Science</topic><topic>Colloids</topic><topic>Mass distribution</topic><topic>Mass spectra</topic><topic>Mass spectroscopy</topic><topic>Nanostructured Systems and Materials</topic><topic>NMR</topic><topic>Nuclear magnetic resonance</topic><topic>Oligomers</topic><topic>Physical Chemistry</topic><topic>Polymerization</topic><topic>Progressions</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kim, I. P.</creatorcontrib><creatorcontrib>Benderskii, V. A.</creatorcontrib><creatorcontrib>Martynenko, V. M.</creatorcontrib><creatorcontrib>Chernyak, A. V.</creatorcontrib><collection>CrossRef</collection><jtitle>High energy chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kim, I. P.</au><au>Benderskii, V. A.</au><au>Martynenko, V. M.</au><au>Chernyak, A. V.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Study of fluoroalkylsilanes, a new class of amphiphilic oligomers: Determination of end groups and chain length</atitle><jtitle>High energy chemistry</jtitle><stitle>High Energy Chem</stitle><date>2017-07-01</date><risdate>2017</risdate><volume>51</volume><issue>4</issue><spage>277</spage><epage>284</epage><pages>277-284</pages><issn>0018-1439</issn><eissn>1608-3148</eissn><abstract>Radiation-initiated polymerization of tetrafluoroethylene (TFE) in the liquid alkylsilanes Si(CH
3
)
4
(I), C
2
H
5
Si(CH
3
)
3
(II), and ClSi(CH
3
)
3
(III) produces fluoroalkylsilane oligomers with the general formula R(C
2
F
4
)
n
X, where X = H or Cl in I, II, and III and R is one of the radicals generated by the abstraction of H from the methyl and ethyl groups in I and II or Cl detachment from III. The nature of R has been determined using an NMR technique, and the molecular mass distribution (MMD) has been found from abundances in anion progressions in mass spectra and from DTG and GPC data. At initial TFE concentrations (
C
0
) changed from 0.4, 1, and 0.13 to 1, 2.7, and 0.7 mol/L in I, II and III, respectively, the average chain length 〈
n
〉 increases from 4–5 to 10–12 and the MMD changes from the unimodal to the bimodal pattern in which the proportion of oligomers with
n
< 6 decreases with increasing
C
0
. As 〈
n
〉 increases and the MMD changes, the homogeneous solution becomes colloidal and then turns into a gel. The colloidal particles are largely composed of long oligomers, and the number of solvent molecules per C
2
F
4
unit decreases with an increase in
C
0
and is 4–7 in the gel.</abstract><cop>Moscow</cop><pub>Pleiades Publishing</pub><doi>10.1134/S0018143917040063</doi><tpages>8</tpages></addata></record> |
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language | eng |
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source | SpringerLink Journals - AutoHoldings |
subjects | Chains (polymeric) Chemistry Chemistry and Materials Science Colloids Mass distribution Mass spectra Mass spectroscopy Nanostructured Systems and Materials NMR Nuclear magnetic resonance Oligomers Physical Chemistry Polymerization Progressions |
title | Study of fluoroalkylsilanes, a new class of amphiphilic oligomers: Determination of end groups and chain length |
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