Antimicrobial Equipment of Poly(Isoprene) Applying Thiol-ene Chemistry

被引:10
|
作者
Kienberger, Julia [1 ]
Noormofidi, Nadja [1 ]
Muehlbacher, Inge [2 ]
Klarholz, Ingo [3 ]
Harms, Carsten [3 ]
Slugovc, Christian [1 ]
机构
[1] Graz Univ Technol, Inst Chem & Technol Mat, A-8010 Graz, Austria
[2] Polymer Competence Ctr Leoben GmbH PCCL, A-8700 Leoben, Austria
[3] TTZ Bremerhaven, D-27572 Bremerhaven, Germany
关键词
anionic polymerization; biological applications of polymers; contact biocides; heteroatom containing polymers; thiol-ene reaction; FREE-RADICAL ADDITION; ANTIBACTERIAL ACTIVITY; QUATERNARY AMMONIUM; POLYMER; COPOLYMERS; BIOCIDES;
D O I
10.1002/pola.26001
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The functionalization of anionically polymerized isoprene with cysteamine applying the thiol-ene reaction is reported. Antimicrobial activity is implemented by quaternization of the amino functionality by either alkylation or by protonation. The resulting polymers were tested against Gram-positive as well as Gram-negative bacteria strains according to the Japanese Industrial Standard Z2801:2000 protocol, partly revealing excellent biocidal performance. Thermal stability up to 200 degrees C allows extrusion processing of the functionalized poly(isoprene)s. The best performing polymer, that is, bearing butylated ammonium-groups, was compounded with the commodity material poly(propylene). The compound bearing 5 wt % of the biocidal polymer exhibited satisfactory biocidal properties. (C) 2012 Wiley Periodicals, Inc. J PolymSci Part A: Polym Chem 50: 2236-2243, 2012
引用
收藏
页码:2236 / 2243
页数:8
相关论文
共 50 条
  • [31] Thiol-ene chemistry for the synthesis and modification of branched organosilicon polymers
    Son, David
    Rissing, Christiana
    Chen, Li
    Andersson, Theodore
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2010, 240
  • [32] Photochemical Functionalization of Graphene Oxide by Thiol-Ene Click Chemistry
    Pineiro-Garcia, Alexis
    Vega-Diaz, Sofia M.
    Tristan, Ferdinando
    Meneses-Rodriguez, David
    Labrada-Delgado, Gladis Judith
    Semetey, Vincent
    INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 2020, 59 (29) : 13033 - 13041
  • [33] Thiol-ene chemistry as an effective tool for hydrophobization of cotton fabrics
    Anna Szymańska
    Marcin Przybylak
    Hieronim Maciejewski
    Agnieszka Przybylska
    Cellulose, 2022, 29 : 1231 - 1247
  • [34] Biofunctional Silicon Nanoparticles by Means of Thiol-Ene Click Chemistry
    Ruizendaal, Loes
    Pujari, Sidharam P.
    Gevaerts, Veronique
    Paulusse, Jos M. J.
    Zuilhof, Han
    CHEMISTRY-AN ASIAN JOURNAL, 2011, 6 (10) : 2776 - 2786
  • [35] Effects of modulus and surface chemistry of thiol-ene photopolymers in nanoimprinting
    Hagberg, Erik C.
    Malkoch, Michael
    Ling, Yibo
    Hawker, Craig J.
    Carter, Kenneth R.
    NANO LETTERS, 2007, 7 (02) : 233 - 237
  • [36] Silicon-thioether dendrimers synthesized with thiol-ene chemistry
    Rissing, Christiana J.
    Son, David Y.
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2009, 237
  • [37] Applications of thiol-ene and thiolyne chemistry for peptide stapling and bioconjugation
    Gonzalez, Ines Rabadan
    McLean, Joshua
    Ostrovitsa, Nikitas
    Fitzgerald, Sheila
    Mezzeta, Andrea
    Guazzelli, Lorenzo
    O'Shea, Donal
    Scanlan, Eoin
    JOURNAL OF PEPTIDE SCIENCE, 2024, 30
  • [38] Functional block copolymers via thiol-ene click chemistry
    Killops, Kato L.
    Gupta, Nalini
    Dimitriou, Michael D.
    Lynd, Nathaniel A.
    Jung, Hyunjung
    Bang, Joona
    Campos, Luis M.
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2011, 242
  • [39] Thiol-ene chemistry as an effective tool for hydrophobization of cotton fabrics
    Szymanska, Anna
    Przybylak, Marcin
    Maciejewski, Hieronim
    Przybylska, Agnieszka
    CELLULOSE, 2022, 29 (02) : 1231 - 1247
  • [40] DNA microarrays on silicon surfaces through thiol-ene chemistry
    Escorihuela, Jorge
    Jose Banuls, Maria
    Puchades, Rosa
    Maquieira, Angel
    CHEMICAL COMMUNICATIONS, 2012, 48 (15) : 2116 - 2118