Absorption Spectrum and Raman Spectroscopy of Coumarin507 Dye Laser in Different Solvents

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Coumarin dye laser compounds are often used as components in coloring agents and sprays., as well as in the odorization of foods. Therefore, the important of these compounds in many felids leading to growth of several ways aiming to advance the control of pharmaceutical and superficial producing. Solvents play an important role in changing the character of coumarin. The investigated spectral properties, as well as the effect of changing the solvent on this property, have been published. results referred that the molar electronic transition energy increased with decreasing the maximum absorption wavelength, and the highest intensity of the absorption spectrum was in the case of acetone solvent. In addition, many bands appear in Raman shift attributed to the ''C=O'' band, ''O=C–O, C–C'', and ''C–O'' deformation. The characteristic vibrations involving the ''O-H'' group is the stretching and bending modes of the ''O-H'' and ''C-O'' parts.

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February 2023

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[1] A.P. de Silva, T.P. Vance, M.E. West, G.D. Wright, Bright molecules with sense, logic, numeracy and utility, Org Biomol Chem. 6 (2008) 2468-2480.

DOI: 10.1039/b802963f

Google Scholar

[2] J. Mannekutla, B. Mulimani, S. Inamdar, Solvent effect on absorption and fluorescence spectra of coumarin laser dyes: evaluation of ground and excited state dipole moments, Spectrochim Acta A Mol Biomol Spectrosc. 69 (2008) 419-426.

DOI: 10.1016/j.saa.2007.04.016

Google Scholar

[3] R.M.L. Christie, Chih-Hung, Studies of fluorescent dyes: part 1. An investigation of the electronic spectral properties of substituted coumarins, Dyes Pigm. 42 (1999) 85-93.

DOI: 10.1016/s0143-7208(99)00012-1

Google Scholar

[4] J. Sokołowska, W. Czajkowski, R. Podsiadły, The photostability of some fluorescent disperse dyes derivatives of coumarin, Dyes Pigm. 49 (2001) 187-191.

DOI: 10.1016/s0143-7208(01)00018-3

Google Scholar

[5] L. Liu, Y. Sun, S. Wei, X. Hu, Y. Zhao, J. Fan, Solvent effect on the absorption and fluorescence of ergone: Determination of ground and excited state dipole moments, Spectrochim Acta A Mol Biomol Spectrosc. 86 (2012) 120-123.

DOI: 10.1016/j.saa.2011.10.016

Google Scholar

[6] S.A. Patil, P.S. Kadolkar, M.N. Wari, S.R. Inamdar, Photo-physical study of coumarins in aqueous organic solvents: an experimental and theoretical approach, Mater. Today Commun. 29 (2021) 102733.

DOI: 10.1016/j.mtcomm.2021.102733

Google Scholar

[7] S. Ramsey, T. Mayo, S. Lambrakos, Novel Optical Systems, Methods, and Applications XXIII, SPIE2020, pp.183-190.

Google Scholar

[8] S. Bagchi, Solvation in homogeneous and heterogeneous media, J Indian Chem Soc. 98 (2021) 100071.

Google Scholar

[9] C. Reichardt, T. Welton, Solvents and solvent effects in organic chemistry, John Wiley & Sons (2011).

Google Scholar

[10] I.F. Al-sharuee, Thermal Conductivity Performance of Silica Aerogel after Exposition on Different Heating under Ambient Pressure, Baghdad Sci J. 16 (2019) 0770-0770.

DOI: 10.21123/bsj.2019.16.3(suppl.).0770

Google Scholar

[11] C. Reichardt, Solvation Effects in Organic Chemistry: A Short Historical Overview, J Org Chem. 87 (2022) 1616-1629. 10.1021/acs.joc.1c01979.

DOI: 10.1021/acs.joc.1c01979

Google Scholar

[12] I.K. Mohammed, Study of Solvent Effects on the Uv/Visible Spectra of A Newly Synthesized Azo-Dye5-(8-Quinaldinolazo)-Para Phenyl Acetic Acid, Indian J F Med Tox. 13 (2019).

DOI: 10.5958/0973-9130.2019.00416.x

Google Scholar

[13] K.H. Ibnaouf, A.O. Elzupir, M.S. AlSalhi, A.S. Alaamer, Influence of functional groups on the photophysical properties of dimethylamino chalcones as laser dyes, Opt Mater. 76 (2018) 216-221.

DOI: 10.1016/j.optmat.2017.12.034

Google Scholar

[14] I. Georgieva, T. Zahariev, A.J. Aquino, N. Trendafilova, H. Lischka, Energy transfer mechanism in luminescence Eu (III) and Tb (III) complexes of coumarin-3-carboxylic acid: A theoretical study, Spectrochim. Acta A Mol Biomol Spectrosc. 240 (2020) 118591.

DOI: 10.1016/j.saa.2020.118591

Google Scholar

[15] C. Maridevarmath, L. Naik, G. Malimath, Dielectric, Photophysical, Solvatochromic, and DFT Studies on Laser Dye Coumarin 334, BrJPh. 49 (2019) 151-160.

DOI: 10.1007/s13538-018-00628-3

Google Scholar

[16] S. Nad, H. Pal, Photoinduced electron transfer from aliphatic amines to coumarin dyes, J chem phy. 116 (2002) 1658-1670.

DOI: 10.1063/1.1415451

Google Scholar

[17] H.M. Fahmy, H.M. Kandel, H.A. Al-Shamiri, N.A. Negm, A.H. Elwahy, M.T. Abou Kana, Spectroscopic Study of Solvent Polarity on the Optical and Photo-Physical Properties of Novel 9, 10-bis (coumarinyl) anthracene, J Fluoresc. 28 (2018) 1421-1430.

DOI: 10.1007/s10895-018-2317-1

Google Scholar

[18] P. Bhavya, R. Melavanki, R. Kusanur, K. Sharma, V. Muttannavar, L. Naik, Effect of viscosity and dielectric constant variation on fractional fluorescence quenching analysis of coumarin dye in binary solvent mixtures, Luminescence. 33 (2018) 933-940.

DOI: 10.1002/bio.3492

Google Scholar

[19] M.A. Musa, J.S. Cooperwood, M.O.F. Khan, A review of coumarin derivatives in pharmacotherapy of breast cancer, Curr Med Chem. 15 (2008) 2664-2679.

DOI: 10.2174/092986708786242877

Google Scholar

[20] W.A. Woldie, Characterization of Dairy Waste Whey and Its' Utilization for the Production of Ethanol, Am J Chem Eng. 9 (2021) 112-118.

Google Scholar

[21] O. Destanoğlu, İ. AteŞ, Determination and evaluation of methanol, ethanol and higher alcohols in legally and illegally produced alcoholic beverages, J Turkish Chem Soc, Sec A: Chem. 6 (2019) 21-28.

DOI: 10.18596/jotcsa.481384

Google Scholar

[22] K. Sridhar, R. Murali, S.M. Younus, K.M. Lakshmi, Computerised Simulation of Spark Ignition Internal Combustion Engine, IOSR J Mech Civil Eng. (2013) 05-14p.

DOI: 10.9790/1684-0530514

Google Scholar

[23] Z. Wang, C. Wang, Is breath acetone a biomarker of diabetes? A historical review on breath acetone measurements, J Breath Res. 7 (2013) 037109.

DOI: 10.1088/1752-7155/7/3/037109

Google Scholar

[24] I.F. AL-Sharuee, Specifications study of Hydrophobic Silica Aerogel Doped with Rhodamine 6G Prepared via Sub-Critical Drying Technique, Iraqi J Sci. (2021) 483-489.

DOI: 10.24996/ijs.2021.62.2.14

Google Scholar

[25] J. Catalán, J.L.G. de Paz, C. Reichardt, On the molecular structure and UV/vis spectroscopic properties of the solvatochromic and thermochromic pyridinium-N-phenolate betaine dye B30, J Phy Chem A. 114 (2010) 6226-6234.

DOI: 10.1021/jp1009302

Google Scholar

[26] S. Zhu, H. Bao, H. Zhang, H. Fu, Q. Zhao, L. Zhou, Y. Li, W. Cai, Optimal excitation wavelength for surface-enhanced Raman spectroscopy: the role of chemical interface damping, J Phy Chem Lett. 12 (2021) 11014-11021.

DOI: 10.1021/acs.jpclett.1c03535

Google Scholar

[27] R. Pikl, C. Fickert, W. Kiefer, Vibrational analysis and normal coordinate analysis of trimethylphosphane, Fresenius J Anal Chem. 355 (1996) 351-353.

DOI: 10.1007/s0021663550351

Google Scholar

[28] N. Colthup, L. Daly, S. Wiberley, Introduction to Infrared and Raman Spectroscopy,Academic Press, New York,, (1990).

Google Scholar

[29] N.C. D Lin-Vien, WG Fateley, JG Grasselli The Handbook of Infrared and Raman Characteristic Frequencies of Organic Molecules, Academic Press San Diego New York Boston London Sydney Tokyo Toronto1991.

DOI: 10.1016/b978-0-08-057116-4.50005-5

Google Scholar