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Experimental and theoretical studies on o-, m- and p-chlorobenzylideneaminoantipyrines.
Three antipyrine derivatives of o-, m- and p-chlorobenzylideneaminoantipyrines were characterized by spectral techniques and density functional calculations. The optimized configurations are veryExpand
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Synthesis, characterization and biological activity of triorganotin 2-phenyl-1,2,3-triazole-4-carboxylates.
The triorganotin 2-phenyl-1,2,3-triazole-4-carboxylates, 2-PhC2N3CO2SnR3 (R=C6H5, 1; c-C6H11, 2; C6H5C(CH3)2CH2, 3), have been prepared and characterized by means of elemental analysis, IR and NMRExpand
  • 93
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Synthesis, vibrational spectral and nonlinear optical studies of N-(4-hydroxy-phenyl)-2-hydroxybenzaldehyde-imine: a combined experimental and theoretical investigation.
The study of imine-bridged organics has been the one hot spot of photo-responsive material sciences in recent years. Herein we make a study of the synthesis, characteristics and potential applicationExpand
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Experimental and density functional studies on 4-(3,4-dihydroxybenzylideneamino)antipyrine, and 4-(2,3,4-trihydroxybenzylideneamino)antipyrine
Abstract Two antipyrine derivates, 4-(3,4-dihydroxybenzylideneamino)antipyrine (DHBAP), and 4-(2,3,4-trihydroxybenzylideneamino)antipyrine (THBAP), are structurally similar Schiff bases derived fromExpand
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Vibrational spectroscopic study of o-, m- and p-hydroxybenzylideneaminoantipyrines.
Three structurally similar antipyrine derivatives of o-hydroxybenzylideneaminoantipyrine (o-HBAP), m-hydroxybenzylideneaminoantipyrine (m-HBAP) and p-hydroxybenzylideneaminoantipyrine (p-HBAP) wereExpand
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Experimental and density functional studies on 4-(2,3-dichlorobenzylideneamino)-antipyrine and 4-(2,5-dichlorobenzylideneamino)antipyrine
Two antipyrine derivates, both with formula C18H15Cl2N3O, are structurally similar Schiff bases derived from the condensation of 2,3-dichlorobenzaldehyde or 2,5-dichlorbenzaldehyde withExpand
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Additive-assisted control over phase-separated nanostructures by manipulating alkylthienyl position at donor backbone for solution-processed, non-fullerene, all-small-molecule solar cells.
  • J. Huang, X. Wang, +6 authors J. Yao
  • Materials Science, Medicine
  • ACS applied materials & interfaces
  • 3 March 2014
A non-fullerene, all-small-molecule solar cell (NF-SMSC) device uses the blend of a small molecule donor and a small molecule acceptor as the active layer. Aggregation ability is a key factor forExpand
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Structural, proton-transfer, thermodynamic and nonlinear optical studies of (E)-2-((2-hydroxyphenyl)iminiomethyl)phenolate.
Recently, the study of imine-bridged organics is interested in proton-transfer and photo-responsive material fields. Herein, we make a investigation on the structural, thermodynamic and nonlinearExpand
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Experimental and theoretical studies on 4-(2,4-dichlorobenzylideneamino)antipyrine and 4-(2,6-dichlorobenzylideneamino)antipyrine.
Two antipyrine derivates, with the same formula C(18)H(15)Cl(2)N(3)O, are structurally similar Schiff bases derived from the condensation of 2,4-dichlorobenzaldehyde or 2,6-dichlorobenzaldehyde andExpand
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Synthesis, structural characterization and cytotoxic activity of diorganotin(IV) complexes of N‐(5‐halosalicylidene)‐α‐amino acid
Four new diorganotin(IV) complexes of N-(5-halosalicylidene)tryptophane, R2Sn[5-X-2-OC6H3CHNCH(CH2Ind)COO] [Ind = 3-indolyl; R, X = Et, Cl (1); Et, Br(2); n-Bu, Cl (3); n-Bu, Br (4)], wereExpand
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