GB787344A - Improvements in and relating to polyamides derived from -a-amino acid n-carboanhydrides - Google Patents

Improvements in and relating to polyamides derived from -a-amino acid n-carboanhydrides

Info

Publication number
GB787344A
GB787344A GB642/55A GB64255A GB787344A GB 787344 A GB787344 A GB 787344A GB 642/55 A GB642/55 A GB 642/55A GB 64255 A GB64255 A GB 64255A GB 787344 A GB787344 A GB 787344A
Authority
GB
United Kingdom
Prior art keywords
carboanhydride
phenyl
styrene
prepared
ammonia
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
GB642/55A
Inventor
Basil Alexander Ripley-Duggan
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Distillers Co Yeast Ltd
Distillers Co Ltd
Original Assignee
Distillers Co Yeast Ltd
Distillers Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority to NL104979D priority Critical patent/NL104979C/xx
Application filed by Distillers Co Yeast Ltd, Distillers Co Ltd filed Critical Distillers Co Yeast Ltd
Priority to GB642/55A priority patent/GB787344A/en
Priority to FR1145293D priority patent/FR1145293A/en
Publication of GB787344A publication Critical patent/GB787344A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G69/00Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
    • C08G69/02Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids
    • C08G69/08Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids derived from amino-carboxylic acids
    • C08G69/10Alpha-amino-carboxylic acids

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Polyamides (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

Abstract

The condensation of a -amino acid N-carboanhydrides is initiated with a polymeric material formed by the polymerization of ethylenically unsaturated monomers which contain as the anhydride condensation-initiating group a primary or secondary amino group, the graft or block type copolymers produced being recovered. Specified a -amino acid N-carboanhydrides are DL-valine-N-carboanhydride, DL - phenyl - alanine - N - carboanhydride or DL - a - amino isobutyric acid - N - carboanhydride. The initiators may be prepared by polymerizing ethylenically unsaturated monomers in the presence of ammonia or a primary amine. Specified unsaturated monomers are styrene, vinyl toluene, methyl and ethyl methacrylates, acrylic acid and esters thereof, vinyl chloride, vinyl acetate, vinylidene chloride, butadiene, acrylonitrile, methacrylo nitrile or epoxy-containing alkyl esters of unsaturated aliphatic acids, e.g. glycidyl methacrylate. In the examples: (1) D L-valine-N-carboanhydride is condensed in the presence of an initiator prepared by polymerizing styrene in liquid ammonia containing sodium as a catalyst; (2) DL-phenyl - alanine - N - carboanhydride is condensed in the presence of a co-oplymerization product of styrene and glycidyl methacrylate prepared using benzoyl peroxide as catalyst which had been reacted with anhydrous ammonia; (3) DL-b -phenyl-analine-N-carboanhydride and DL-a -aminoisobutyric acid N-carboanhydride are condensed with the initiator of Example (2); (4) a copolymer of styrene and glycidyl acrylate prepared by heating the two reactants in the presence of a ,a -azo-diisobutyronitrile as catalyst is reacted with ammonia and used as initiator in the condensation of DL-phenyl - alanine - N - carboanhydride. The products are thermoplastic and may be moulded into transparent sheets. Specifications 653,597, 675,298 and U.S.A. Specifications 2,592,447, 2,644,808 and 2,657,972 are referred to.
GB642/55A 1955-01-08 1955-01-08 Improvements in and relating to polyamides derived from -a-amino acid n-carboanhydrides Expired GB787344A (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
NL104979D NL104979C (en) 1955-01-08
GB642/55A GB787344A (en) 1955-01-08 1955-01-08 Improvements in and relating to polyamides derived from -a-amino acid n-carboanhydrides
FR1145293D FR1145293A (en) 1955-01-08 1956-01-06 Process for the preparation of graft copolymers

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB642/55A GB787344A (en) 1955-01-08 1955-01-08 Improvements in and relating to polyamides derived from -a-amino acid n-carboanhydrides
GB1145293X 1955-01-08

Publications (1)

Publication Number Publication Date
GB787344A true GB787344A (en) 1957-12-04

Family

ID=29422080

Family Applications (1)

Application Number Title Priority Date Filing Date
GB642/55A Expired GB787344A (en) 1955-01-08 1955-01-08 Improvements in and relating to polyamides derived from -a-amino acid n-carboanhydrides

Country Status (3)

Country Link
FR (1) FR1145293A (en)
GB (1) GB787344A (en)
NL (1) NL104979C (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3252966A (en) * 1961-06-23 1966-05-24 Gevaert Photo Prod Nv Preparation of block and graft copolymers by photopolymerization in the presence of a photosensitizing dyestuff and a reducing agent
WO1999064495A1 (en) * 1998-06-05 1999-12-16 Ústav Makromolekulární Chemie Akademie Věd České Republiky FUNCTIONALISED POLYMERS OF α-AMINO ACIDS AND THE METHOD OF PREPARATION THEREOF

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3252966A (en) * 1961-06-23 1966-05-24 Gevaert Photo Prod Nv Preparation of block and graft copolymers by photopolymerization in the presence of a photosensitizing dyestuff and a reducing agent
WO1999064495A1 (en) * 1998-06-05 1999-12-16 Ústav Makromolekulární Chemie Akademie Věd České Republiky FUNCTIONALISED POLYMERS OF α-AMINO ACIDS AND THE METHOD OF PREPARATION THEREOF

Also Published As

Publication number Publication date
NL104979C (en)
FR1145293A (en) 1957-10-24

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