TY - JOUR
T1 - Self-assembled supramolecular films derived from marine deoxyribonucleic acid (DNA) - Cationic surfactant complexes
T2 - Large-scale preparation and optical and thermal properties
AU - Wang, L.
AU - Yoshida, J.
AU - Ogata, N.
AU - Sasaki, S.
AU - Kajiyama, T.
N1 - Copyright:
Copyright 2011 Elsevier B.V., All rights reserved.
PY - 2001
Y1 - 2001
N2 - Series of polyelectrolyte - surfactant complexes, DNA - cationic surfactant complexes (cetyltrimethylammonium, cetylpyridinium, and cetylbenzyldimethylammonium), and their self-assembled bulk film materials were prepared on a large scale. Circular dichroism (CD) analysis indicated that the right-handed double helix structure of DNA was retained in these bulk film materials. TGA analysis suggested that 4 molecules of water were required to retain the B-type conformation of the DNA helix in the self-assembled bulk film materials. In addition, it revealed that DNA and the DNA - surfactant complex film materials were thermostable up to as high as 180°C. Thermodynamical analysis indicated that these film materials were thermo-extensive over a temperature range from 100 to 148°C. The DNA conformation in the supramolecular complex films can be reversibly tuned by changing the environmental humidity. Film formation was found to occur by self-assembly and self-organization with evaporation of solvent molecules. Various functional dyes such as laser dye, NLO dye, and photochromic dye could easily be incorporated in the self-assembled supramolecular complex films as adducts. Studies of the induced CD spectra demonstrated that 4[4-(dimethylamino)styryl]-1-dococylpyridinium (DMASDPB) could orient on the chiral nanotemplates of DNA in the self-assembled films. UV - vis analysis indicated that these film materials have high transparency from 300 to about 1000 nm. These self-assembled functional-dye-containing DNA - surfactant complex materials, with good processability for multilayer integration into large-area devices, will have promising applications in molecular optical and molecular optoelectronic fields.
AB - Series of polyelectrolyte - surfactant complexes, DNA - cationic surfactant complexes (cetyltrimethylammonium, cetylpyridinium, and cetylbenzyldimethylammonium), and their self-assembled bulk film materials were prepared on a large scale. Circular dichroism (CD) analysis indicated that the right-handed double helix structure of DNA was retained in these bulk film materials. TGA analysis suggested that 4 molecules of water were required to retain the B-type conformation of the DNA helix in the self-assembled bulk film materials. In addition, it revealed that DNA and the DNA - surfactant complex film materials were thermostable up to as high as 180°C. Thermodynamical analysis indicated that these film materials were thermo-extensive over a temperature range from 100 to 148°C. The DNA conformation in the supramolecular complex films can be reversibly tuned by changing the environmental humidity. Film formation was found to occur by self-assembly and self-organization with evaporation of solvent molecules. Various functional dyes such as laser dye, NLO dye, and photochromic dye could easily be incorporated in the self-assembled supramolecular complex films as adducts. Studies of the induced CD spectra demonstrated that 4[4-(dimethylamino)styryl]-1-dococylpyridinium (DMASDPB) could orient on the chiral nanotemplates of DNA in the self-assembled films. UV - vis analysis indicated that these film materials have high transparency from 300 to about 1000 nm. These self-assembled functional-dye-containing DNA - surfactant complex materials, with good processability for multilayer integration into large-area devices, will have promising applications in molecular optical and molecular optoelectronic fields.
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U2 - 10.1021/cm000869g
DO - 10.1021/cm000869g
M3 - Article
AN - SCOPUS:0034838523
VL - 13
SP - 1273
EP - 1281
JO - Chemistry of Materials
JF - Chemistry of Materials
SN - 0897-4756
IS - 4
ER -