scholarly journals Photomobile polymers from commercially available compounds: photoinduced deformation of side-chain polymers containing hydrogen-bonded photoreactive compounds

2012 ◽  
Vol 44 (5) ◽  
pp. 410-414 ◽  
Author(s):  
Mizuho Kondo ◽  
Masahiko Takemoto ◽  
Ryohei Fukae ◽  
Nobuhiro Kawatsuki
Keyword(s):  
Side Chain ◽  
Hydrogen Bonded

Dielectric properties of a hydrogen-bonded liquid-crystalline side-chain polymer

1995 ◽  
Vol 16 (10) ◽  
pp. 733-739 ◽  
Author(s):  
Kazuo Araki ◽  
Takashi Kato ◽  
Uday Kumar ◽  
Jean M. J. Fréchet
Keyword(s):  
Dielectric Properties ◽  
Liquid Crystalline ◽  
Side Chain ◽  
Chain Polymer ◽  
Hydrogen Bonded

The ST pinch: A side chain-to-side chain hydrogen-bonded motif

2012 ◽  
Vol 80 (5) ◽  
pp. 1259-1263 ◽  
Author(s):  
Martha G. Bomar ◽  
Upadhyayula S. Raghavender ◽  
Alexander W. I. Spindel ◽  
Krishna Kodukula ◽  
Amit K. Galande
Keyword(s):  
Side Chain ◽  
Hydrogen Bonded

Poly(4-vinylpyridine)-based hydrogen bonded side-chain liquid crystal polymers

2008 ◽  
Vol 68 (6) ◽  
pp. 1097-1102 ◽  
Author(s):  
Xiangen Han ◽  
Subing Zhang ◽  
Robert A. Shanks ◽  
Dumitru Pavel
Keyword(s):  
Liquid Crystal ◽  
Side Chain ◽  
Liquid Crystal Polymers ◽  
Hydrogen Bonded

Hierarchical Structures of Hydrogen-Bonded Liquid-Crystalline Side-Chain Diblock Copolymers in Nanoparticles

2012 ◽  
Vol 45 (21) ◽  
pp. 8743-8751 ◽  
Author(s):  
Antti J. Soininen ◽  
Antti Rahikkala ◽  
Juuso T. Korhonen ◽  
Esko I. Kauppinen ◽  
Raffaele Mezzenga ◽  
...  
Keyword(s):  
Liquid Crystalline ◽  
Diblock Copolymers ◽  
Hierarchical Structures ◽  
Side Chain ◽  
Hydrogen Bonded

Synthesis of chalcone-containing methacrylate-based hydrogen bonded side chain liquid crystalline polymer and its dielectric properties

2015 ◽  
Vol 28 (11) ◽  
pp. 1351-1356 ◽  
Author(s):  
Burak Korkmaz ◽  
Yesim Hepuzer Gursel ◽  
Nimet Yilmaz Canli ◽  
Zeynep Güven Özdemir ◽  
Mustafa Okutan ◽  
...  
Keyword(s):  
Dielectric Properties ◽  
Liquid Crystalline Polymer ◽  
Liquid Crystalline ◽  
Crystalline Polymer ◽  
Side Chain ◽  
Hydrogen Bonded

A water wire inL-prolyl-L-serine monohydrate

2013 ◽  
Vol 69 (5) ◽  
pp. 556-559 ◽  
Author(s):  
Carl Henrik Görbitz ◽  
Vitthal N. Yadav
Keyword(s):  
Title Compound ◽  
Functional Group ◽  
Crystal Packing ◽  
Side Chain ◽  
Propanoic Acid ◽  
Water Molecules ◽  
Packing Arrangement ◽  
Hydroxy Groups ◽  
Hydrogen Bonded

Despite the extra functional group in the serine side chain, the crystal packing arrangement of the title compound {systematic name: (S)-3-hydroxy-2-[(S)-pyrrolidine-2-carboxamido]propanoic acid monohydrate}, C8H14N2O4·H2O, is essentially the same as observed for a series of L-Pro-L-Nop peptide hydrates, where Nop is a strictly nonpolar residue. This is rendered possible by a monoclinicP21packing arrangement withZ′ = 2 that deviates from orthorhombicP212121symmetry only for the seryl hydroxy groups, which form infinite O—H...O—H hydrogen-bonded chains along the 5.3 Åaaxis. At the same time, cocrystallized water molecules form parallel water wires.

Crystal structure of 2-Methyl-2-(2,4,5-trichlorophenoxy)propionic acid

1982 ◽  
Vol 35 (10) ◽  
pp. 2145
Author(s):  
CHL Kennard ◽  
G Smith ◽  
WL Duax ◽  
DC Swenson
Keyword(s):  
Crystal Structure ◽  
Propionic Acid ◽  
Direct Methods ◽  
Chain Conformation ◽  
Side Chain ◽  
Acid Form ◽  
Side Chain Conformation ◽  
Phenoxyacetic Acids ◽  
Hydrogen Bonded

The crystal structure of 2-methyl-2-(2,4,5-trichlorophenoxy)propionic acid was determined. C10H9Cl3O3, Mv 283.5, triclinic, P1, a 9.859(2), b 11.542(2), c 6.247(1) �, α(100.13(2), β 97.26(2), γ 114.68(2)�, pc 1.52 g cm-3, Z 2, F(000) 288, μ (CuKα) 66.1 cm-1. It was solved by direct methods and refined to a final R of 0.051 for 1249 observed reflections. The molecules of the acid form the usual hydrogen bonded cyclic dimers [O. . .O,2.638(5) �] and have the synplanar-synplanar (carbonyl) side-chain conformation common to the phenoxyacetic acids and 2-phenoxypropionic acids but different from previous determinations of phenoxyisobutyric acid analogues.

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