Molecular Dynamic, Hirshfeld Surface, Computational Quantum and Spectroscopic analysis of 4-Hydroxy-1-Naphthaldehyde

IF 0.9 Q4 CHEMISTRY, PHYSICAL
M. Mir, M. Jassal, K. Andrews
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引用次数: 0

Abstract

Computational Quantum and Spectroscopic analysis of 4-Hydroxy-1-Naphthaldehyde Known also as 4-Hydroxynaphthalene-1-carbaldehyde, 4-hydroxy-1-naphthaldehyde (4H1NA) is a crucial precursor of many coordinating agents. A commercial compound called 4-hydroxy-1-naphthaldehyde (4H1NA) can be used to make a number of different sensors. In the development of many chemosensors, they operate effectively as a functionalized fluorescent backbone. Molecular Dynamic, Hirshfeld Surface, Computational Quantum analysis of Naphthaldehyde. The methods employed in the analysis of the compound involve the DFT calculations, using DFT method and B3LYP/6-311++G (d, p) basis set with respect to its FTIR, NMR, and UV-Visible spectrum. The NMR chemical shifts of carbon and protons in CDCl3 was determined by GIAO method. For the molecule of reference, HOMO-LUMO and Donor-Acceptor interactions were also taken into consideration. Investigations also looked into ELF, Fukui activity, and nonlinear optical properties. The investigation of the compound at its atomic level was analysed using the computational methods so that chemical, medicinal, and environmental research make use of them to make the molecule more in an improved form with distinguished properties. Strong interaction has been produced as a result of electron transfer from the oxygen atoms lone pair LP (2) to the anti-bonding orbital *(C3-C5) with a significant stabilization energy of 42.61kcal/mol. The attributes of the NLO molecule were calculated and found to be superior to those of the urea molecule, with linear and first order hyper polarizability situation. Our findings imply that the reference molecule can be a heavier contender for NLO as a surface material and could be considered as a vital substance for medicine purpose in the drug industry due to its maximum electrophilicity index. A commercial compound called 4-hydroxy-1-naphthaldehyde (4H1NA) can be used to make a number of different sensors. The compound has good structural and optical properties. They can be employed for a variety of optical limiting applications because of their unusual optical characteristic, which exhibits third-order nonlinear behavior.
4-羟基-1-萘醛的分子动力学,Hirshfeld表面,计算量子和光谱分析
4-羟基-1-萘醛(4 -羟基-1-萘醛,4H1NA)是许多配位剂的重要前体。一种叫做4-羟基-1-萘醛(4H1NA)的商业化合物可以用来制造许多不同的传感器。在许多化学传感器的发展中,它们作为一种功能化的荧光骨架有效地发挥作用。分子动力学,赫斯菲尔德表面,萘醛的计算量子分析。化合物的分析方法包括DFT计算,使用DFT方法和B3LYP/6-311++G (d, p)基集对其FTIR、NMR和uv -可见光谱进行分析。用GIAO法测定了CDCl3中碳和质子的核磁共振化学位移。作为参比分子,还考虑了HOMO-LUMO和供体-受体相互作用。调查还研究了ELF、福井活动和非线性光学性质。在原子水平上对化合物的研究使用计算方法进行了分析,以便化学、医学和环境研究利用它们使分子更加具有改进的形式和独特的性质。氧原子孤对LP(2)向反键轨道*(C3-C5)转移电子产生了强相互作用,稳定能达到42.61kcal/mol。计算了NLO分子的性质,发现NLO分子的性质优于尿素分子,具有线性和一阶超极化情况。我们的研究结果表明,参考分子可以成为NLO作为表面材料的更有力的竞争者,并且由于其最大的亲电性指数,可以被认为是制药工业中用于医学目的的重要物质。一种叫做4-羟基-1-萘醛(4H1NA)的商业化合物可以用来制造许多不同的传感器。该化合物具有良好的结构性能和光学性能。由于其独特的光学特性,具有三阶非线性特性,可用于各种光学限制应用。
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来源期刊
Current Organocatalysis
Current Organocatalysis CHEMISTRY, PHYSICAL-
CiteScore
2.00
自引率
0.00%
发文量
28
期刊介绍: Current Organocatalysis is an international peer-reviewed journal that publishes significant research in all areas of organocatalysis. The journal covers organo homogeneous/heterogeneous catalysis, innovative mechanistic studies and kinetics of organocatalytic processes focusing on practical, theoretical and computational aspects. It also includes potential applications of organocatalysts in the fields of drug discovery, synthesis of novel molecules, synthetic method development, green chemistry and chemoenzymatic reactions. This journal also accepts papers on methods, reagents, and mechanism of a synthetic process and technology pertaining to chemistry. Moreover, this journal features full-length/mini review articles within organocatalysis and synthetic chemistry. It is the premier source of organocatalysis and synthetic methods related information for chemists, biologists and engineers pursuing research in industry and academia.
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