Mandal Tripti, Dey Arka, Pathak Sudipta, Islam Md Maidul, Konar Saugata, Ortega-Castro Joaquín, Seth Saikat Kumar, Ray Partha Pratim, Frontera Antonio, Mukhopadhyay Subrata
Department of Chemistry, Jadavpur University Jadavpur Kolkata 700032 India.
Department of Condensed Matter Physics and Material Sciences, S. N. Bose National Centre for Basic Sciences Block JD, Sec. III, Salt Lake Kolkata 700106 India.
RSC Adv. 2019 Mar 27;9(17):9663-9677. doi: 10.1039/c9ra00666d. eCollection 2019 Mar 22.
Three salts [perchlorate (2), chloride (3) and tetrafluoroborate (4)] were synthesized from a 1-(2-aminoethyl)-6-hydroxy-2-oxo-1,2-dihydro-[4,4'-bipyridine]-3,5-dicarbonitrile compound (1) and characterized by spectroscopic and single crystal X-ray diffraction methods. Various noncovalent interactions (, anion⋯π, π⋯π, lp⋯π) are explored in the solid state crystal structure of the salts. Optical band gaps of all the four compounds were determined from their solid-state UV-vis spectrum. Electrical properties like electrical conductivity, photosensitivity, were calculated and the results revealed that they have potential to act as optoelectronic devices. The values of the electrical parameters increase several times when they are exposed to visible light rather than in dark conditions. The light sensing properties of the salts (2-4) are enhanced compared to that of the mother organic compound 1 but the magnitude of this enhancement is not same for the three salts. This observation has been rationalized by theoretical considerations. Moreover, the DNA binding ability of one of the representative salts (compound 2) was examined to check the biological importance of the synthesized salts.
由1-(2-氨基乙基)-6-羟基-2-氧代-1,2-二氢-[4,4'-联吡啶]-3,5-二甲腈化合物(1)合成了三种盐[高氯酸盐(2)、氯化物(3)和四氟硼酸盐(4)],并通过光谱和单晶X射线衍射方法对其进行了表征。在盐的固态晶体结构中探索了各种非共价相互作用(,阴离子⋯π,π⋯π,孤对电子⋯π)。根据四种化合物的固态紫外-可见光谱测定了它们的光学带隙。计算了电导率、光敏性等电学性质,结果表明它们具有作为光电器件的潜力。当它们暴露在可见光下而不是在黑暗条件下时,电学参数的值会增加几倍。与母体有机化合物(1)相比,盐(2-4)的光传感性能有所增强,但三种盐的增强幅度并不相同。这一观察结果已通过理论考虑得到合理解释。此外,还研究了一种代表性盐(化合物2)的DNA结合能力,以检验合成盐的生物学重要性。