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Journal

2015 | 13 | 1 |

Article title

Synthesis, Photo-sensitive and Electrochemical Properties of Rod-like Aromatic Aldehyde with Azo Bridge

Content

Title variants

Languages of publication

EN

Abstracts

EN

Publisher

Journal

Year

Volume

13

Issue

1

Physical description

Dates

received
10 - 12 - 2014
online
5 - 8 - 2015
accepted
9 - 6 - 2015

Contributors

author
  • School of Chemistry and Chemical Engineering, Xianyang Normal University, Shaanxi, China
author
  • School of Chemistry and Chemical Engineering, Xianyang Normal University, Shaanxi, China
author
  • School of Chemistry and Chemical Engineering, Xianyang Normal University, Shaanxi, China

References

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  • [2] Kilincarslan R., Erdem E., Synthesis and spectral characterization of some new azo dyes and their metal complexes, Transition Met. Chem., 2007, 32, 102-106
  • [3] Dabbagh H.A., Teimouri A., Insertion reaction of azidosulfonyl azo dye with model alicyclic and heterocyclic compounds, Russ. J. Org. Chem., 2008, 44, 1464–1470[WoS]
  • [4] Kashanian S., Zeidali S.H., Omidfar K., Shahabadi N., Multi-spectroscopic DNA interaction studies of sunset yellow food additive, Mol Biol Rep., 2012, 39, 10045-10050[WoS][Crossref]
  • [5] Singh A.K., Das J., Majumdar N., Novel bacteriorhodopsin analogs based on azo chromophores, J. Am. Chem. Soc., 1996, 118, 6185-6191
  • [6] Nieto G., Huvaere K., Skibsted L.H., Antioxidant activity of rosemary and thyme by-products and synergism with added antioxidant in a liposome system, Eur Food Res Technol., 2011, 233, 11-18[WoS]
  • [7] Nagaveni N.G., Royb A., Prasad V., Achiral bent-core azo compounds: effect of different types of linkage groups and their direction of linking on liquid crystalline properties, J. Mater. Chem., 2012, 22, 8948-8959[Crossref][WoS]
  • [8] Kay E.R., Leigh D.A., Zerbetto F., Synthetic molecular motors and mechanical machines, Angew. Chem., 2007, 119, 72-196[Crossref][WoS]
  • [9] Balzani V., Credi A., Venturi M., Light powered molecular machines, Chem. Soc. Rew., 2009, 38, 1542-1550
  • [10] Silva A.P.D., Gunarane H.Q.N., Rice T.E., Signaling recognition events with fluorescent sensors and switches, Chem. Rev., 1997, 97, 1515-1566
  • [11] Ledoux I., Zyss J., Barni E., Barolo C., Diulgheroff N., Quagliotto P., Viscardi G., Properties of novel azodyes containing powerful acceptor groups and thiophene moiety, Synth. Met., 2000, 115, 213–217
  • [12] Urbas A., Tondiglia V., Natarajan L., Sutherland R., Yu H., Li J.H., et al. Optically switchable liquid crystal photonic structures, J. Am. Chem. Soc., 2004, 126, 13580-13581
  • [13] Newton J., Walton H., Coles H., Hodge P., New LMM organosiloxanes with photoisomerising azo groups, Mol. Cryst. Liq. Cryst., 1995, 260, 107-125
  • [14] Furumi S., Akiyama H., Morino S., Ichimura K., A convenient preparation of photoactive monolayers for liquid crystal photoalignment by the surface adsorption of an aminoalkylated, J. Mater. Chem., 1998, 8, 65-70[Crossref]
  • [15] Wang J.H., Liu L., Liu G.F., Guo J.X., Jia D.Z., Properties of novel azodyes containing powerful acceptor groups and thiophene moiety, Synth. Met., 2000, 115, 213±217
  • [16] Zhang Y.Q., Ortega J., Baumeister U., Folcia C. L., Sanz-Enguita G., Walker C., et al., Activated carbon modified with 4-(8-hydroxyquinoline-azo)benzamidine for selective solid-phase extraction and preconcentration of trace lead from environmental samples, Microchim Acta, 2010, 171, 225-232[WoS]
  • [17] Nicolescu F.A., Jerca V.V., Dancus I., Petris A., Nicolescu T.V., Rau I.B., et al. Synthesis and characterization of side-chain maleimide-styrene copolymers with new pendant azobenzene moieties, J. Polym. Res., 2011, 18, 1009-1016[WoS][Crossref]
  • [18] Liu J.Q., Zhang Q.Z., Zhang J.Z., Hou, W.G., Photochemical behaviours of star-like liquid crystal with azobenzene terminal groups, J. Mater. Sci., 2005, 40, 4517-4521[Crossref]
  • [19] Wang J.H., Liu L., Liu G.F., Guo J.X., Jia D.Z., Three novel photoisomeric compounds of the 4-acyl pyrazolone derivants: Crystal structures and substituent effects on photo-isomerism in solid state, Sci. Chin. Ser. B: Chem., 2008, 51, 661-668
  • [20] Kašpar M., Novotná V., Hamplová V., Podoliak N., Nonnenmacher D., Glogarová F., et al., Antiferroelectric phase in liquid crystalline compounds containing an azo groups containing an azo group in their molecular core, Liquid crystal, 2011, 38, 309-315
  • [21] Zheng M.Y., An Z.W., Synthesis and mesophase of liquid crystals of multi-ring monoesteryl aryl aldehyde, Chin. J. Appl. Chem., 2007, 24, 396-400, (in Chinese)
  • [22] Chouhary V.R., Dumbre D.K., Narkhede V.S., Solvent-free oxidation of aldehydes to acids by TBHP using environmental-friendly MnO4-1 4 -exchanged Mg-Al hydrotalcite catalyst, J. Chem. Sci., 2012, 124, 835-839
  • [23] Zheng M.Y., An Z.W., Rod-like Schiff Base Magnetic Liquid Crystals Bearing Organic Radical, Chin. J. Chem., 2006, 24, 1754-1757[Crossref]
  • [24] Zou Z.Q., Deng Z.J., Yu X.H., Zhang M.M., Zhao S.H., Luo T., et al. A new facile approach to N-alkylpyrroles from direct redox reaction of 4-hydroxy-L-proline with aldehydes, Sci. Chin. Ser. B: Chem., 2012, 55, 43-49[Crossref]
  • [25] Kuvshinova S.A., Burmistrov V.A., Fokin D.S., Blokhina S.V., Koifman O.I., Thermodynamic Properties and Selectivity of Substituted Liquid-Crystal Formylazobenzenes as Stationary Phases for Gas Chromatography, Anal. Chem., 2009, 64, 505-508[WoS]
  • [26] Arias J., Bardaji M., Espinet P., Folcia C.L., Ortega, J., Etxebarria, J. Azo isocyanide gold(I) liquid crystals, highly birefringent and photosensitive in the mesophase, Inorg. Chem., 2009, 48, 6205-6210[WoS]
  • [27] Xiang N.J., Lee T.H., Leung L.M., So S.K., Shi J.X., Gong M.L., Synthesis and photoluminescence of two novel bipolar organic compounds, Acta Chimica Sinica, 2006, 64, 1157-1162, (in Chinese)
  • [28] Pandey S., Kolli B., Mishra S.P., Samui A.B.S., Siloxane polymers containing azo moieties synthesized by click, J. Polym. Sci. Part A: Polym. Chem., 2012, 50, 1205-1215 [Crossref]

Document Type

Publication order reference

Identifiers

YADDA identifier

bwmeta1.element.-psjd-doi-10_1515_chem-2015-0122
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