化学
单斜晶系
结晶学
吡啶
晶体结构
氢键
轨道能级差
Crystal(编程语言)
拉曼光谱
分子
立体化学
药物化学
有机化学
计算机科学
光学
物理
程序设计语言
作者
Wang Zong,Ke-Lai Chen,Yuting Li,Lin Huang,Peng Xu,Xin-Yi Jiang,Chun‐Lin Ni,Yan-Xian Li,Jin-Ying Liang,Yao-Mou Zhang
标识
DOI:10.1080/00958972.2023.2253973
摘要
AbstractIn this article, we present the syntheses, crystal structures, vibrational spectra, optical and antibacterial properties of two new organic-inorganic hybrids, [Py(CH2)3TPP][CoCl4]·H2O (1) and [Py(CH2)3TPP][CuCl4] (2), where [Py(CH2)3TPP]2+ was 1-(1′-pyridyl-propyl)-3-triphenyl phosphonium. Two hybrids were crystallized in the monoclinic space group P21/n. The hybrids consisted of a [Py(CH2)3TPP]2+ cation and a tetrahedral [CoCl4]2−/[CuCl4]2− anion, where the crystal structure was stabilized by C−H···Cl, O−H···Cl, and C−H···O hydrogen bonds due to the presence of a water molecule in 1, and the crystal structure of 2 was stabilized by C−H···Cl hydrogen bonds. Experimental vibrational bands (IR and Raman) have been discussed and assigned. The intermolecular energy, the energy gap between HOMO and LUMO orbitals, as well as the first hyperpolarizabilities were predicted based on DFT calculations. The low energy gaps (1.26 eV for 1 and 1.20 eV for 2) were responsible for the charge transfer interactions that eventually occur between the cation and anion. The first hyperpolarizabilities (βtot) of 1 and 2 were 82 and 237 times as high as that of the standard KDP crystal, respectively, indicating that the as-prepared hybrids were excellent materials for NLO applications. Furthermore, it was found that both salts exhibit good bactericidal activity against Escherichia coli and Staphylococcus aureus.KEYWORDS: Pyridinium-substituted triphenylphosphoniumtetrachlorocobalt/copper(II)crystal structuresnonlinear optical propertiesantibacterial activity Disclosure statementNo potential conflict of interest was reported by the author(s).Additional informationFundingThis work has been partially supported by the Science and Technology Project (No. 2016A010103025) from Guangdong Science and Technology Department.
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