20262-55-9Relevant articles and documents
Synthesis, crystal structure and electronic applications of monocarboxylic acid substituted phthalonitrile derivatives combined with DFT studies
Tun?, Gülenay,Can?mkurbey, Betül,Dedeo?lu, Burcu,Zorlu, Yunus,Ery?lmaz, Serpil,Gürek, Ay?e Gül
, (2021/05/13)
Monocarboxylic acid substituted phthalonitrile derivatives (PN1 and PN2) have been synthesized and their molecular geometries and hydrogen bond interactions investigated with single cystal X-ray diffraction analysis. PN1-a and PN2 crystal structures linked by a pair of O–H?O hydrogen bonds form classical carboxylic acid inversion dimers, whilst PN1-b crystal structure stabilized by classical O–H?O and O–H?N hydrogen bonding interactions. Spectral characterizations of PN1-a and PN2 structures have been performed by FT-IR, 1H-13C NMR and UV-Vis techniques. Molecular structure optimization and structural properties of PN1 and PN2 in the forms of monomer and dimer have been studied with the DFT approach, B3LYP functional and 6-311++G(d,p) basis set. The effects of dimeric forms of structures on geometrical and spectral parameters have been evaluated together with the values of monomeric forms and experimental ones. Concepts specific to electronic absorption spectra such as absorption wavelengths and major contributions to electronic transitions and FMOs energy values have been determined by TD-DFT approach. Some reactivity properties of the monomer PN1-a and PN2 structures have been evaluated through global, local parameter values and MEP visuals. It was shown that PN2 monomer structure which has both a low HOMO-LUMO energy gap (ΔE=3.83 eV) and a higher chemical softness value (S=0.52 eV?1) is more reactive than PN1-a monomer. The potentials of being nonlinear optical (NLO) material and some thermodynamic parameters that are thought to contribute to their structural properties have been determined theoretically for PN1-a and PN2 monomeric forms. Furthermore, it is determined that PN2 has superior properties compared to PN1 based on the electrical characterization of the compounds.
An expedient and convenient approach for one-pot synthesis of 1H-isoindole-1,3(2H)-diones
Ekhtiari, Zeinab,Havasi, Forugh,Nikpour, Farzad
, p. 941 - 944 (2016/10/13)
An easy and expedient method for the one-pot synthesis of 1H-isoindole-1,3(2H)-diones has been developed by the reaction of the corresponding cyclic anhydrides with guanidinium chloride as a nitrogen source in the presence of FeCl3 as a catalyst under mild reaction conditions.
Visible photostability of some ruthenium and platinum phthalocyanines in water and in the presence of organic substrates
Carchesio, Manuela,Tonucci, Lucia,D'Alessandro, Nicola,Morvillo, Antonino,Boccio, Piero Del,Bressan, Mario
experimental part, p. 499 - 508 (2011/03/18)
Water-soluble, metal-tetrasubstituted phthalocyanines (-SO3H, MPcS and -COOH, MPcC) of platinum and ruthenium were synthesized and their photostability to visible light irradiation was determined. For the ruthenium phthalocyanines, the characte
