Literature DB >> 22117623

Molecular origins of optoelectronic properties in coumarin dyes: toward designer solar cell and laser applications.

Xiaogang Liu1, Jacqueline M Cole, Paul G Waddell, Tze-Chia Lin, Jignesh Radia, Anita Zeidler.   

Abstract

Coumarin derivatives are used in a wide range of applications, such as dye-sensitized solar cells (DSCs) and dye lasers, and have therefore attracted considerable research interest. In order to understand the molecular origins of their optoelectronic properties, molecular structures for 29 coumarin laser dyes are statistically analyzed. To this end, data for 25 compounds were taken from the Cambridge Structural Database and compared with data for four new crystal structures of coumarin laser dyes [Coumarin 487 (C(19)H(23)NO(2)), Coumarin 498 (C(16)H(17)NO(4)S), Coumarin 510 (C(20)H(18)N(2)O(2)), and Coumarin 525 (C(22)H(18)N(2)O(3))], which are reported herein. The competing contributions of different resonance states to the bond lengths of the 4- and 7-substituted coumarin laser dyes are computed based on the harmonic oscillator stabilization energy model. Consequently, a positive correlation between the contribution of the para-quinoidal resonance state and the UV-vis peak absorption wavelength of these coumarins is revealed. Furthermore, the perturbations of optoelectronic properties, owing to chemical substituents in these coumarin laser dyes, are analyzed: it is found that their UV-vis peak absorption and lasing wavelengths experience a red shift, as the electron-donating strength of the 7-position substituent increases and/or the electron-withdrawing strength of the 3- or 4-position substituent rises; this conclusion is corroborated by quantum-chemical calculations. It is also revealed that the closer the relevant substituents align with the direction of the intramolecular charge transfer (ICT), the larger the spectral shifts and the higher the molar extinction coefficients of coumarin laser dyes. These findings are important for understanding the ICT mechanism in coumarins. Meanwhile, all structure-property correlations revealed herein will enable knowledge-based molecular design of coumarins for dye lasers and DSC applications.

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Year:  2011        PMID: 22117623     DOI: 10.1021/jp209925y

Source DB:  PubMed          Journal:  J Phys Chem A        ISSN: 1089-5639            Impact factor:   2.781


  14 in total

1.  Fluorescent 7-Substituted Coumarin Dyes: Solvatochromism and NLO Studies.

Authors:  Archana A Bhagwat; Nagaiyan Sekar
Journal:  J Fluoresc       Date:  2018-10-29       Impact factor: 2.217

2.  Electronic Structure, Optical Properties and Quantum Chemical Investigation on Synthesized Coumarin Derivative in Liquid Media for Optoelectronic Devices.

Authors:  A G Pramod; C G Renuka; Y F Nadaf
Journal:  J Fluoresc       Date:  2019-07-22       Impact factor: 2.217

3.  Coumarin 343 in aqueous solution: theoretical analysis of absorption.

Authors:  Evgeniy S Savenko; Victor V Kostjukov
Journal:  J Mol Model       Date:  2022-04-23       Impact factor: 1.810

4.  Visible-Light Photoinitiation of (Meth)acrylate Polymerization with Autonomous Post-conversion.

Authors:  Kangmin Kim; Jasmine Sinha; Jeffrey W Stansbury; Charles B Musgrave
Journal:  Macromolecules       Date:  2021-08-17       Impact factor: 6.057

5.  Coumarin 6H-fused fluorescent probe for highly sensitive detection of coralyne using oligonucleotide-modified silver nanoparticles.

Authors:  Hatice Müge Usta; Mehrdad Forough; Özgül Persil Çetinkol
Journal:  Anal Bioanal Chem       Date:  2022-08-17       Impact factor: 4.478

6.  Coumarin-based fluorescent probes for H2S detection.

Authors:  Wenhua Li; Wei Sun; Xiaoqiang Yu; Lupei Du; Minyong Li
Journal:  J Fluoresc       Date:  2012-09-23       Impact factor: 2.217

7.  NLOphoric Red Emitting Bis Coumarins with O-BF(2)-O core - Synthesis, Photophysical Properties and DFT Studies.

Authors:  Abhinav B Tathe; Nagaiyan Sekar
Journal:  J Fluoresc       Date:  2015-12-11       Impact factor: 2.217

8.  Solid-state fluorescence emission and second-order nonlinear optical properties of coumarin-based fluorophores.

Authors:  Yi-Feng Sun; He-Ping Wang; Zhi-Yong Chen; Wen-Zeng Duan
Journal:  J Fluoresc       Date:  2012-09-02       Impact factor: 2.217

9.  New 3-Ethynylaryl Coumarin-Based Dyes for DSSC Applications: Synthesis, Spectroscopic Properties, and Theoretical Calculations.

Authors:  João Sarrato; Ana Lucia Pinto; Gabriela Malta; Eva G Röck; João Pina; João Carlos Lima; A Jorge Parola; Paula S Branco
Journal:  Molecules       Date:  2021-05-14       Impact factor: 4.411

10.  Ethyl 2-[(2-oxo-2H-chromen-7-yl)-oxy]acetate.

Authors:  Hoong-Kun Fun; Ching Kheng Quah; Krishnendu Aich; Sangita Das; Shyamaprosad Goswami
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2013-03-06
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