author_facet Sakamoto, Munenori
Kuroyanagi, Yoshimitsu
Sakamoto, Ryuichi
Sakamoto, Munenori
Kuroyanagi, Yoshimitsu
Sakamoto, Ryuichi
author Sakamoto, Munenori
Kuroyanagi, Yoshimitsu
Sakamoto, Ryuichi
spellingShingle Sakamoto, Munenori
Kuroyanagi, Yoshimitsu
Sakamoto, Ryuichi
Journal of Polymer Science: Polymer Chemistry Edition
Multichain copoly(α‐amino acid). II. Preparation and properties of multi‐Nϵ‐poly(γ‐benzyl‐L‐glutamyl)copoly(L‐lysine γ‐methyl‐L‐glutamate)
General Medicine
author_sort sakamoto, munenori
spelling Sakamoto, Munenori Kuroyanagi, Yoshimitsu Sakamoto, Ryuichi 0360-6376 1542-9369 Wiley General Medicine http://dx.doi.org/10.1002/pol.1978.170160817 <jats:title>Abstract</jats:title><jats:p>A number of multi‐<jats:italic>N</jats:italic><jats:sup>ϵ</jats:sup>‐poly(γ‐benzyl‐<jats:sc>L</jats:sc>‐glutamyl)copoly(<jats:sc>L</jats:sc>‐lysine γ‐methyl‐<jats:sc>L</jats:sc>‐glutamate)s with branches having various degrees of polymerization and with various intervals of the grafting sites in the core molecule were prepared in <jats:italic>N</jats:italic>,<jats:italic>N</jats:italic>‐dimethylformamide containing dimethyl sulfoxide by the reaction of <jats:italic>N</jats:italic>‐carboxy anhydride of γ‐benzyl <jats:sc>L</jats:sc>‐glutamate with random copoly(<jats:sc>L</jats:sc>‐lysine γ‐methyl‐<jats:sc>L</jats:sc>‐glutamate)s of different composition with various anhydride‐initiator ratios. The relationship between the intrinsic viscosity measured in a coil solvent, dichloroacetic acid (DCA), and the number‐average molecular weight determined by osmometry was found to be expressed by the Mark–Houwink–Sakurada equation for the multichain copoly(α‐amino acid)s which were made from the same polymeric initiator. The observed α values of the multichain copoly(α‐amino acid)s in the equation were lower than that of linear poly(γ‐benzyl‐<jats:sc>L</jats:sc>‐glutamate). The solvent induced helix–coil transition of the multichain copolymer was investigated in the chloroform‒DCA system by the ORD technique. Two kinds of transition regions were clearly distinguished: The α‐helices of the core molecules underwent the transition at lower DCA concentration and those of the branch chains at higher DCA concentration. The reduced viscosity of the multichain copoly‐(α‐amino acid) increased slightly between the two transition regions, in contrast to the large decrease in the reduced viscosity of linear poly(γ‐benzyl‐<jats:sc>L</jats:sc>‐glutamate) during the helix–coil transition.</jats:p> Multichain copoly(α‐amino acid). II. Preparation and properties of multi‐<i>N</i><sup>ϵ</sup>‐poly(γ‐benzyl‐<scp>L</scp>‐glutamyl)copoly(<scp>L</scp>‐lysine γ‐methyl‐<scp>L</scp>‐glutamate) Journal of Polymer Science: Polymer Chemistry Edition
doi_str_mv 10.1002/pol.1978.170160817
facet_avail Online
format ElectronicArticle
fullrecord blob:ai-49-aHR0cDovL2R4LmRvaS5vcmcvMTAuMTAwMi9wb2wuMTk3OC4xNzAxNjA4MTc
id ai-49-aHR0cDovL2R4LmRvaS5vcmcvMTAuMTAwMi9wb2wuMTk3OC4xNzAxNjA4MTc
institution DE-105
DE-14
DE-Ch1
DE-L229
DE-D275
DE-Bn3
DE-Brt1
DE-D161
DE-Gla1
DE-Zi4
DE-15
DE-Pl11
DE-Rs1
imprint Wiley, 1978
imprint_str_mv Wiley, 1978
issn 0360-6376
1542-9369
issn_str_mv 0360-6376
1542-9369
language English
mega_collection Wiley (CrossRef)
match_str sakamoto1978multichaincopolyaaminoacidiipreparationandpropertiesofmultinpolygbenzyllglutamylcopolyllysinegmethyllglutamate
publishDateSort 1978
publisher Wiley
recordtype ai
record_format ai
series Journal of Polymer Science: Polymer Chemistry Edition
source_id 49
title Multichain copoly(α‐amino acid). II. Preparation and properties of multi‐Nϵ‐poly(γ‐benzyl‐L‐glutamyl)copoly(L‐lysine γ‐methyl‐L‐glutamate)
title_unstemmed Multichain copoly(α‐amino acid). II. Preparation and properties of multi‐Nϵ‐poly(γ‐benzyl‐L‐glutamyl)copoly(L‐lysine γ‐methyl‐L‐glutamate)
title_full Multichain copoly(α‐amino acid). II. Preparation and properties of multi‐Nϵ‐poly(γ‐benzyl‐L‐glutamyl)copoly(L‐lysine γ‐methyl‐L‐glutamate)
title_fullStr Multichain copoly(α‐amino acid). II. Preparation and properties of multi‐Nϵ‐poly(γ‐benzyl‐L‐glutamyl)copoly(L‐lysine γ‐methyl‐L‐glutamate)
title_full_unstemmed Multichain copoly(α‐amino acid). II. Preparation and properties of multi‐Nϵ‐poly(γ‐benzyl‐L‐glutamyl)copoly(L‐lysine γ‐methyl‐L‐glutamate)
title_short Multichain copoly(α‐amino acid). II. Preparation and properties of multi‐Nϵ‐poly(γ‐benzyl‐L‐glutamyl)copoly(L‐lysine γ‐methyl‐L‐glutamate)
title_sort multichain copoly(α‐amino acid). ii. preparation and properties of multi‐<i>n</i><sup>ϵ</sup>‐poly(γ‐benzyl‐<scp>l</scp>‐glutamyl)copoly(<scp>l</scp>‐lysine γ‐methyl‐<scp>l</scp>‐glutamate)
topic General Medicine
url http://dx.doi.org/10.1002/pol.1978.170160817
publishDate 1978
physical 2001-2017
description <jats:title>Abstract</jats:title><jats:p>A number of multi‐<jats:italic>N</jats:italic><jats:sup>ϵ</jats:sup>‐poly(γ‐benzyl‐<jats:sc>L</jats:sc>‐glutamyl)copoly(<jats:sc>L</jats:sc>‐lysine γ‐methyl‐<jats:sc>L</jats:sc>‐glutamate)s with branches having various degrees of polymerization and with various intervals of the grafting sites in the core molecule were prepared in <jats:italic>N</jats:italic>,<jats:italic>N</jats:italic>‐dimethylformamide containing dimethyl sulfoxide by the reaction of <jats:italic>N</jats:italic>‐carboxy anhydride of γ‐benzyl <jats:sc>L</jats:sc>‐glutamate with random copoly(<jats:sc>L</jats:sc>‐lysine γ‐methyl‐<jats:sc>L</jats:sc>‐glutamate)s of different composition with various anhydride‐initiator ratios. The relationship between the intrinsic viscosity measured in a coil solvent, dichloroacetic acid (DCA), and the number‐average molecular weight determined by osmometry was found to be expressed by the Mark–Houwink–Sakurada equation for the multichain copoly(α‐amino acid)s which were made from the same polymeric initiator. The observed α values of the multichain copoly(α‐amino acid)s in the equation were lower than that of linear poly(γ‐benzyl‐<jats:sc>L</jats:sc>‐glutamate). The solvent induced helix–coil transition of the multichain copolymer was investigated in the chloroform‒DCA system by the ORD technique. Two kinds of transition regions were clearly distinguished: The α‐helices of the core molecules underwent the transition at lower DCA concentration and those of the branch chains at higher DCA concentration. The reduced viscosity of the multichain copoly‐(α‐amino acid) increased slightly between the two transition regions, in contrast to the large decrease in the reduced viscosity of linear poly(γ‐benzyl‐<jats:sc>L</jats:sc>‐glutamate) during the helix–coil transition.</jats:p>
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author Sakamoto, Munenori, Kuroyanagi, Yoshimitsu, Sakamoto, Ryuichi
author_facet Sakamoto, Munenori, Kuroyanagi, Yoshimitsu, Sakamoto, Ryuichi, Sakamoto, Munenori, Kuroyanagi, Yoshimitsu, Sakamoto, Ryuichi
author_sort sakamoto, munenori
container_issue 8
container_start_page 2001
container_title Journal of Polymer Science: Polymer Chemistry Edition
container_volume 16
description <jats:title>Abstract</jats:title><jats:p>A number of multi‐<jats:italic>N</jats:italic><jats:sup>ϵ</jats:sup>‐poly(γ‐benzyl‐<jats:sc>L</jats:sc>‐glutamyl)copoly(<jats:sc>L</jats:sc>‐lysine γ‐methyl‐<jats:sc>L</jats:sc>‐glutamate)s with branches having various degrees of polymerization and with various intervals of the grafting sites in the core molecule were prepared in <jats:italic>N</jats:italic>,<jats:italic>N</jats:italic>‐dimethylformamide containing dimethyl sulfoxide by the reaction of <jats:italic>N</jats:italic>‐carboxy anhydride of γ‐benzyl <jats:sc>L</jats:sc>‐glutamate with random copoly(<jats:sc>L</jats:sc>‐lysine γ‐methyl‐<jats:sc>L</jats:sc>‐glutamate)s of different composition with various anhydride‐initiator ratios. The relationship between the intrinsic viscosity measured in a coil solvent, dichloroacetic acid (DCA), and the number‐average molecular weight determined by osmometry was found to be expressed by the Mark–Houwink–Sakurada equation for the multichain copoly(α‐amino acid)s which were made from the same polymeric initiator. The observed α values of the multichain copoly(α‐amino acid)s in the equation were lower than that of linear poly(γ‐benzyl‐<jats:sc>L</jats:sc>‐glutamate). The solvent induced helix–coil transition of the multichain copolymer was investigated in the chloroform‒DCA system by the ORD technique. Two kinds of transition regions were clearly distinguished: The α‐helices of the core molecules underwent the transition at lower DCA concentration and those of the branch chains at higher DCA concentration. The reduced viscosity of the multichain copoly‐(α‐amino acid) increased slightly between the two transition regions, in contrast to the large decrease in the reduced viscosity of linear poly(γ‐benzyl‐<jats:sc>L</jats:sc>‐glutamate) during the helix–coil transition.</jats:p>
doi_str_mv 10.1002/pol.1978.170160817
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id ai-49-aHR0cDovL2R4LmRvaS5vcmcvMTAuMTAwMi9wb2wuMTk3OC4xNzAxNjA4MTc
imprint Wiley, 1978
imprint_str_mv Wiley, 1978
institution DE-105, DE-14, DE-Ch1, DE-L229, DE-D275, DE-Bn3, DE-Brt1, DE-D161, DE-Gla1, DE-Zi4, DE-15, DE-Pl11, DE-Rs1
issn 0360-6376, 1542-9369
issn_str_mv 0360-6376, 1542-9369
language English
last_indexed 2024-03-01T15:00:15.694Z
match_str sakamoto1978multichaincopolyaaminoacidiipreparationandpropertiesofmultinpolygbenzyllglutamylcopolyllysinegmethyllglutamate
mega_collection Wiley (CrossRef)
physical 2001-2017
publishDate 1978
publishDateSort 1978
publisher Wiley
record_format ai
recordtype ai
series Journal of Polymer Science: Polymer Chemistry Edition
source_id 49
spelling Sakamoto, Munenori Kuroyanagi, Yoshimitsu Sakamoto, Ryuichi 0360-6376 1542-9369 Wiley General Medicine http://dx.doi.org/10.1002/pol.1978.170160817 <jats:title>Abstract</jats:title><jats:p>A number of multi‐<jats:italic>N</jats:italic><jats:sup>ϵ</jats:sup>‐poly(γ‐benzyl‐<jats:sc>L</jats:sc>‐glutamyl)copoly(<jats:sc>L</jats:sc>‐lysine γ‐methyl‐<jats:sc>L</jats:sc>‐glutamate)s with branches having various degrees of polymerization and with various intervals of the grafting sites in the core molecule were prepared in <jats:italic>N</jats:italic>,<jats:italic>N</jats:italic>‐dimethylformamide containing dimethyl sulfoxide by the reaction of <jats:italic>N</jats:italic>‐carboxy anhydride of γ‐benzyl <jats:sc>L</jats:sc>‐glutamate with random copoly(<jats:sc>L</jats:sc>‐lysine γ‐methyl‐<jats:sc>L</jats:sc>‐glutamate)s of different composition with various anhydride‐initiator ratios. The relationship between the intrinsic viscosity measured in a coil solvent, dichloroacetic acid (DCA), and the number‐average molecular weight determined by osmometry was found to be expressed by the Mark–Houwink–Sakurada equation for the multichain copoly(α‐amino acid)s which were made from the same polymeric initiator. The observed α values of the multichain copoly(α‐amino acid)s in the equation were lower than that of linear poly(γ‐benzyl‐<jats:sc>L</jats:sc>‐glutamate). The solvent induced helix–coil transition of the multichain copolymer was investigated in the chloroform‒DCA system by the ORD technique. Two kinds of transition regions were clearly distinguished: The α‐helices of the core molecules underwent the transition at lower DCA concentration and those of the branch chains at higher DCA concentration. The reduced viscosity of the multichain copoly‐(α‐amino acid) increased slightly between the two transition regions, in contrast to the large decrease in the reduced viscosity of linear poly(γ‐benzyl‐<jats:sc>L</jats:sc>‐glutamate) during the helix–coil transition.</jats:p> Multichain copoly(α‐amino acid). II. Preparation and properties of multi‐<i>N</i><sup>ϵ</sup>‐poly(γ‐benzyl‐<scp>L</scp>‐glutamyl)copoly(<scp>L</scp>‐lysine γ‐methyl‐<scp>L</scp>‐glutamate) Journal of Polymer Science: Polymer Chemistry Edition
spellingShingle Sakamoto, Munenori, Kuroyanagi, Yoshimitsu, Sakamoto, Ryuichi, Journal of Polymer Science: Polymer Chemistry Edition, Multichain copoly(α‐amino acid). II. Preparation and properties of multi‐Nϵ‐poly(γ‐benzyl‐L‐glutamyl)copoly(L‐lysine γ‐methyl‐L‐glutamate), General Medicine
title Multichain copoly(α‐amino acid). II. Preparation and properties of multi‐Nϵ‐poly(γ‐benzyl‐L‐glutamyl)copoly(L‐lysine γ‐methyl‐L‐glutamate)
title_full Multichain copoly(α‐amino acid). II. Preparation and properties of multi‐Nϵ‐poly(γ‐benzyl‐L‐glutamyl)copoly(L‐lysine γ‐methyl‐L‐glutamate)
title_fullStr Multichain copoly(α‐amino acid). II. Preparation and properties of multi‐Nϵ‐poly(γ‐benzyl‐L‐glutamyl)copoly(L‐lysine γ‐methyl‐L‐glutamate)
title_full_unstemmed Multichain copoly(α‐amino acid). II. Preparation and properties of multi‐Nϵ‐poly(γ‐benzyl‐L‐glutamyl)copoly(L‐lysine γ‐methyl‐L‐glutamate)
title_short Multichain copoly(α‐amino acid). II. Preparation and properties of multi‐Nϵ‐poly(γ‐benzyl‐L‐glutamyl)copoly(L‐lysine γ‐methyl‐L‐glutamate)
title_sort multichain copoly(α‐amino acid). ii. preparation and properties of multi‐<i>n</i><sup>ϵ</sup>‐poly(γ‐benzyl‐<scp>l</scp>‐glutamyl)copoly(<scp>l</scp>‐lysine γ‐methyl‐<scp>l</scp>‐glutamate)
title_unstemmed Multichain copoly(α‐amino acid). II. Preparation and properties of multi‐Nϵ‐poly(γ‐benzyl‐L‐glutamyl)copoly(L‐lysine γ‐methyl‐L‐glutamate)
topic General Medicine
url http://dx.doi.org/10.1002/pol.1978.170160817