Synthesis of Naphtho-[2,3]-furan derivatives for investigative insights into solvatochromic behaviour

被引:3
|
作者
Ali, Sonia
Kaur, Khushwinder [1 ]
Agarwal, Jyoti [1 ]
机构
[1] Panjab Univ, Dept Chem, Chandigarh 160014, India
关键词
Naphthofuran; Solvatochromism; Gaussian study; TGA analysis; Absorption and Fluorescence spectroscopy; STATE DIPOLE-MOMENTS; PHOTOPHYSICAL PROPERTIES; SOLVENT POLARITY; DESIGN;
D O I
10.1016/j.molliq.2023.121256
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The paper delineates the synthesis of naphtho-[2,3]-furan derivatives (viz. a viz. naphtho-[2,3]-furan-3-yl acetate (NF), 9-nitronaphtho-[2,3]-furan-3-yl acetate (NNF) and 9-bromonaphtho-[2,3-]-furan-3-yl acet-ate (BNF)) using a multistep approach. The products were obtained in high yields and characterized by FT-IR, 1H NMR, 13C NMR, and HRMS spectroscopy. The absorption and fluorescence spectra of these derivatives were recorded in the solvent of different polarities. Solvatochromic correlations were employed to estimate ground state (lg) and excited state (le) dipole moments. The results suggested higher stability of molecules in the singlet excited state than in the ground state. Theoretical investiga-tions indicated that the AEHUMO-LUMO gap varied as AENF> AEBNF >AENNF. The thermogravimetric analysis (TGA) confirmed the higher stability of NNF as compared to BNF and NF.(c) 2023 Elsevier B.V. All rights reserved.
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页数:8
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