TY - JOUR
T1 - Functionalization of boron nitride nanosheets (BNNSs) by organic polymers
T2 - formation of substituted polythiophene–BNNS structures
AU - Petrelli, Christopher
AU - Goos, Alan
AU - Ruhlandt-Senge, Karin
AU - Spencer, James T.
N1 - Publisher Copyright:
© 2016, Springer Science+Business Media New York.
PY - 2016/5/1
Y1 - 2016/5/1
N2 - Recent experiments with hexagonal boron nitride (h-BN) have shown the successful covalent and non-covalent functionalization of these boron nitride nanostructures, especially nanosheets (BNNS). This paper explores the synthesis of several thiophene-based polymers with conjugated pendant groups and their reactions with BNNSs. Specifically, two phenyl carboxylic acid functionalized polythiophene polymers, poly[3-(4-methoxycarbonylphenyl)thiophene] and poly[3-(4-benzoic acid)thiophene], have been prepared and reacted with exfoliated BNNSs. The resulting complexes between the conjugated polythiophene polymers and the BNNS are reported and characterized by their reaggregation stability and by spectroscopic methods.
AB - Recent experiments with hexagonal boron nitride (h-BN) have shown the successful covalent and non-covalent functionalization of these boron nitride nanostructures, especially nanosheets (BNNS). This paper explores the synthesis of several thiophene-based polymers with conjugated pendant groups and their reactions with BNNSs. Specifically, two phenyl carboxylic acid functionalized polythiophene polymers, poly[3-(4-methoxycarbonylphenyl)thiophene] and poly[3-(4-benzoic acid)thiophene], have been prepared and reacted with exfoliated BNNSs. The resulting complexes between the conjugated polythiophene polymers and the BNNS are reported and characterized by their reaggregation stability and by spectroscopic methods.
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U2 - 10.1007/s10853-016-9800-3
DO - 10.1007/s10853-016-9800-3
M3 - Article
AN - SCOPUS:84959240240
SN - 0022-2461
VL - 51
SP - 4952
EP - 4962
JO - Journal of Materials Science
JF - Journal of Materials Science
IS - 10
ER -