79887-16-4Relevant articles and documents
Highly ordered smectic structures of disc-rod luminescent liquid crystals: The role of the tolane group
Liu, Yurong,Li, Wei,Zhou, Xuan,Wong, Wai-Yeung,Yu, Zhen-Qiang
, p. 3555 - 3561 (2021/03/26)
Two novel calamitic tolane luminogen-modified triphenylene-based discotic luminescent liquid-crystals (LLC) were rationally designed and synthesized to investigate the self-assembly competition between triphenylene discogens and tolane calamitic mesogens.
A concise synthesis of isoxazole-based side chain of Micafungin
Rao, Pallavi,Hussain, Ismail,Rao, Venkataramanarao,Sen, Saikat,Oruganti, Srinivas
supporting information, p. 2180 - 2187 (2019/06/25)
A concise synthesis of key isoxazole-based side chain of Micafungin, an USFDA approved anti-fungal agent, has been delineated. The route design notably involves a one pot regioselective isoxazole construction from the corresponding aryl aldehyde and alkyne intermediates.
Cleavage of the Carbon–Carbon Triple Bonds of Arylacetylenes for the Synthesis of Arylnitriles without a Metal Catalyst
Lin, Yuanguang,Song, Qiuling
, p. 3056 - 3059 (2016/07/12)
Cleavage of the carbon–carbon triple bonds of alkynes was achieved, which led to the synthesis of arylnitriles under transition-metal-free conditions. A vast range of terminal alkyne substrates underwent this reaction to provide the corresponding nitriles in moderate to good yields with good functional group tolerance.
Synthesis of some novel aromatic alkynyl silanes: Mesomorphic characterization of ethynyl-substituted rod-shaped molecules
Srinivasa,Hariprasad
, p. 17 - 27 (2014/01/17)
The synthesis and characterization of 10 new rod-shaped substituted benzoates possessing the 4-(2-trimethylsilyl)ethynyl group in terminal phenyl position is reported employing the simple and efficient Sonogashira cross-coupling and DCC esterification. 4′
Aerobic oxynitration of alkynes with tBuONO and TEMPO
Dutta, Uttam,Maity, Soham,Kancherla, Rajesh,Maiti, Debabrata
, p. 6302 - 6305 (2015/02/19)
An efficient method for stereoselective nitroaminoxylation of alkyne has been reported. The reaction enjoys a broad substrate scope, good functional group tolerance, and high yields. Synthetically useful α-nitroketones can be accessed through these products in a single step.
Synthesis of diphenyl-diacetylene-based nematic liquid crystals and their high birefringence properties
Arakawa, Yuki,Nakajima, Shunpei,Ishige, Ryohei,Uchimura, Makoto,Kang, Sungmin,Konishi, Gen-Ichi,Watanabe, Junji
, p. 8394 - 8398 (2012/07/28)
We synthesized two series of diphenyl-diacetylene (DPDA)-based materials with alkoxy and alkyl tails of length m (DPDA-OCm and DPDA-Cm, respectively), and measured their nematic-phase birefringence (Δn) as a function of wavelength and temperature. We found that Δn decreases with an increase in m, possibly by a dilution effect of the low-Δn alkyl tail. Further, of the two series, Δn was found to be relatively higher in the DPDA-OCm materials, with the highest value of 0.4 obtained for DPDA-OC1 at 550 nm at 10 °C below the isotropic-to-nematic transition temperature. Further, we observed the temperature dependence for Δn, which is proportional to the order parameter (s). From extrapolation to s = 1 (the perfect orientation state), it is speculated that the DPDA-O moiety has the potential to afford a very large Δn of 0.9. The Royal Society of Chemistry 2012.
High birefringence nematic liquid crystals for display and telecom applications
Catanescu, Carmen Otilia,Chien,Wu, Shin-Tson
, p. 93/[1135]-102/[1144] (2007/10/03)
Several compounds with high birefringence and, having tolane structure were synthesized. For a high polarizability, isothiocyanato (NCS) terminal group was introduced. Another goal of this study was reduction of melting point and smectic phases by introduction of fluorine as lateral substituent. The transition temperatures for all the synthesized compounds and the refractive and dielectric indices for one of the compounds have been determined. Electro-optic (EO) measurements were also performed.
Ordering of apolar and polar solutes in nematic solvents
Dingemans,Photinos,Samulski,Terzis,Wutz
, p. 7046 - 7061 (2007/10/03)
To illustrate the relative importance of electrostatic interactions, the LC-NMR data for a pair of polar and apolar solutes that are structural isomers, ortho- and para-dichlorobenzene, respectively, dissolved in polar and apolar nematogens were analyzed.
Synthesis and mesomorphic properties of some fluorinated benzoate liquid crystals
Yang, Yong Gang,Chen,Tang,Wen
, p. 1 - 15 (2007/10/03)
Three series of [4-(4′-n-alkyloxyphenyl)acetylenyl]-2,6- difluorophenyl fluorinated benezoates and one series of fluorinated benzoates with 2,3,5,6-tetrafluorophenylene group and semi-perfluorocarbon chain have been synthesized. Their phase transition temperatures have been measured by texture observation in a polarizing microscope and confirmed by DSC. For the series without fluorocarbon chains, increasing the quantity of fluorosubstituents on the terminal phenyl groups decreased nematic stability (TN-I), but the breadth of the SmA phase range was increased. Lateral fluorosubstitution in the central group lowered the nematic stability (TN-I) and decreased the breadth of the SmA phase range. The series with semiperfluorocarbon chains were more likely to form SmA phases than the series with hydrogencarbon chains, and with the increasing of fluorosubstituents quantity on the terminal phenyl groups nematic and SmA stability (TN-I and TsmA-N) were both decreased.
High birefringence phenylacetylene liquid crystals with low viscosity
Sekine, Chizu,Fujisawa, Koichi,Iwakura, Kazunori,Minai, Masayoshi
, p. 711 - 718 (2007/10/03)
We have synthesized new high Δ n 3-ring phenylacetylene(3PA) liquid crystals which have substituent groups with core center phenyl ring and investigated the effects of substitution on physical properties. Nematic range and viscosity were improved remarkab
