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11. |
2‐Hydroxy‐3‐ionene chloride |
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Journal of Polymer Science: Polymer Chemistry Edition,
Volume 13,
Issue 3,
1975,
Page 693-700
G. K. Noren,
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摘要:
AbstractThe condensation of dimethylamine with epichlorohydrin gave an almost quantitative yield of 2‐hydroxy‐3‐dimethylaminopropyl chloride which was polymerized via the Menschutkin reaction to give 2‐hydroxy‐3‐ionene chloride. This cationically charged polymer was obtained in greater than 90% yields as a white to tan solid when precipitated into acetone. Number‐average molecular weights of up to 10,000 and intrinsic viscosities of up to 0.11 dl/g in 0.4Mpotassium bromide were found. These low molecular weights were attributed to several impurities that were identified as being produced by side reactions. Thermal analysis of the polymers showed an endothermic transition at 32–39°C with the onset of decomposition occurin
ISSN:0360-6376
DOI:10.1002/pol.1975.170130311
出版商:John Wiley&Sons, Inc.
年代:1975
数据来源: WILEY
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12. |
Polymers from 4,4′‐thiodiphenol |
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Journal of Polymer Science: Polymer Chemistry Edition,
Volume 13,
Issue 3,
1975,
Page 701-706
C. Samyn,
C. S. Marvel,
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摘要:
AbstractPolyesters were made with aromatic diacid chlorides and 4,4,‐thiodiphenol. Isophthaloyl chloride and/or terephthaloyl chloride were used as acid chlorides alone or together with 5‐cyanoisophthaloyl chloride or [2.2]p‐cyclophane‐3,9‐dicarboxylic acid chloride. The latter components were incorporated in order to make the polymers useful for crosslinking. A polyether could be obtained by polycondensation of 2,4‐dichloro‐benzonitrile and 4,4′‐thiodiphenol. The polycondensations were run in nitrob
ISSN:0360-6376
DOI:10.1002/pol.1975.170130312
出版商:John Wiley&Sons, Inc.
年代:1975
数据来源: WILEY
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13. |
Polymerization of methacrylates. I. Polymerization reactivity of picryl methacrylate |
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Journal of Polymer Science: Polymer Chemistry Edition,
Volume 13,
Issue 3,
1975,
Page 707-716
Yoshinori Kadoma,
Takashi Toida,
Kenji Takeda,
Keikichi Uno,
Yoshio Iwakura,
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摘要:
AbstractThe polymerization of picryl (PMA), 2,4‐dinitrophenyl (2,4‐DNMA),2,6‐dinitrophenyl (2,6‐DNMA), 2‐methyl‐4,6‐dinitrophenyl (MDNMA), and 2,6‐dimethylphenyl methacrylates (DMMA) was carried out in benzene at 60°C. PMA, 2,6‐DNMA, and MDNMA did not undergo radical homopolymerization, while 2,4‐DNMA and DMMA did. The results suggest that the growing radical readily attacks the oxygen atom of the nitro group at the 2 position of the terminal phenyl group due to the steric effect of the substituent at the 6 position, resulting in chain termination. PMA formed a charge‐transfer complex with 2‐naphthyl methacrylate (NMA). The stoichiometric composition of this complex was shown to be 1:1 molar complex. PMA was readily copolymerized with NMA. The amount of solvent affected the composition of the copolymer obtained at a given same mole fraction in feed. The results suggest that charge‐transfer interaction between the ester groups affects the
ISSN:0360-6376
DOI:10.1002/pol.1975.170130313
出版商:John Wiley&Sons, Inc.
年代:1975
数据来源: WILEY
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14. |
Singlet oxygen and polymer photooxidations. I. Sensitizers, quenchers, and reactants |
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Journal of Polymer Science: Polymer Chemistry Edition,
Volume 13,
Issue 3,
1975,
Page 717-736
A. Zweig,
W. A. Henderson,
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摘要:
AbstractA study designed to ascertain the role of singlet molecular oxygen in the photodegradation of plastics established that most classes of dye chromophores are sensitizers in polymer films, absorbing light and transferring the absorbed energy to ambient triplet ground state molecular oxygen, generating metastable reactive singlet molecular oxygen. Unsaturated polymers containing polybutadiene, polyisoprene, etc. are highly reactive to singlet oxygen produced through photosensitization, generating hydroxylic and carbonyl derivatives and losing their rubbery properties as consequences of such reactions. Many types of transition metal chelates are singlet oxygen quenchers. The relationships of the structures and spectroscopic properties of these chelates to their efficiency in quenching singlet oxygen are examined and discussed.
ISSN:0360-6376
DOI:10.1002/pol.1975.170130314
出版商:John Wiley&Sons, Inc.
年代:1975
数据来源: WILEY
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15. |
Mechanical surface activation beneath reactive adhesives (SABRA) as effective pretreatment for adhesive bonding |
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Journal of Polymer Science: Polymer Chemistry Edition,
Volume 13,
Issue 3,
1975,
Page 737-740
Chaim H. Lerchenthal,
Manual Brenman,
Nobert Yits'haq,
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ISSN:0360-6376
DOI:10.1002/pol.1975.170130315
出版商:John Wiley&Sons, Inc.
年代:1975
数据来源: WILEY
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16. |
Photopolymerization ofN,N‐bis(2‐cyanoethyl)acrylamide |
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Journal of Polymer Science: Polymer Chemistry Edition,
Volume 13,
Issue 3,
1975,
Page 741-744
C. Azuma,
N. Ogata,
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ISSN:0360-6376
DOI:10.1002/pol.1975.170130316
出版商:John Wiley&Sons, Inc.
年代:1975
数据来源: WILEY
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17. |
Reduction of polymers by use of complex metal hydrides (III) |
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Journal of Polymer Science: Polymer Chemistry Edition,
Volume 13,
Issue 3,
1975,
Page 745-748
H. L. Cohen,
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ISSN:0360-6376
DOI:10.1002/pol.1975.170130317
出版商:John Wiley&Sons, Inc.
年代:1975
数据来源: WILEY
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18. |
Polyamides and polyesters derived from 1,1,3‐trimethyl‐3‐(p‐aminophenyl)‐5‐indanamine and 1,1,3‐trimethyl‐3‐(p‐hydroxyphenyl)‐5‐indanol |
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Journal of Polymer Science: Polymer Chemistry Edition,
Volume 13,
Issue 3,
1975,
Page 749-754
John C. Wilson,
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ISSN:0360-6376
DOI:10.1002/pol.1975.170130318
出版商:John Wiley&Sons, Inc.
年代:1975
数据来源: WILEY
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19. |
Estimation of the purity of graft copolymers by thin‐layer chromatography |
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Journal of Polymer Science: Polymer Chemistry Edition,
Volume 13,
Issue 3,
1975,
Page 755-760
Fumitaka Horii,
Yoshito Ikada,
Ichiro Sakurada,
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ISSN:0360-6376
DOI:10.1002/pol.1975.170130319
出版商:John Wiley&Sons, Inc.
年代:1975
数据来源: WILEY
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