Generic placeholder image

Letters in Organic Chemistry

Editor-in-Chief

ISSN (Print): 1570-1786
ISSN (Online): 1875-6255

Research Article

Spectroscopic and Computational Studies on a Dansyl Based Luminescent Probe: Detection of Water Contaminant in Hygroscopic Deuterated Solvents

Author(s): Saurodeep Mandal, Koushik Pramanik , Sujoy Das, Md Majharul Islam, Sukhendu Mandal and Prithidipa Sahoo*

Volume 19, Issue 1, 2022

Published on: 10 June, 2021

Page: [71 - 82] Pages: 12

DOI: 10.2174/1570178618666210610161531

Price: $65

Abstract

A Dansyl functionalized fluorescent probe (DFFP) has been intended, synthesized, and well-characterized (NMR, IR, Mass, SEM, SCXRD), capable of sensing trace amounts of water contaminant in hygroscopic deuterated solvents by changing colour under UV irradiation. A distinct bathochromic shift in emission spectra of probe DFFP and the visual colour change (Green to Yellow) under UV lamp are the key evidence of the presence of water contaminant. To prove the potentiality of the probe while detecting the remnant water, we did some experimental studies along with exhaustive theoretical evaluation. DFT (Energy optimization and other calculations) helped in better understanding the sensing mechanism and the mode of interactions among probe-water-solvent. Total electron density mapped over Electrostatic Potential Surface and calculation of ESP charges helped in locating more electron-dense regions in the ground state. The involvement of TD-DFT studies helped in finding the possible electronic transitions and corresponding absorption bands. Moreover, the probe is capable of sensing ethanolic water vapour in the gaseous phase. Due to high fluorescence and being nontoxic to cells, probe DFFP could be used as a potential cell imaging dye. It has been employed in a human cancer cell line (A549), and fluorescent confocal microscopic images were obtained.

Keywords: Chemosensor, detection of remnant water, deuterated solvents, cell imaging fluorescence dye, fluorescence decay, water contaminant in organic solvents.

Graphical Abstract
[1]
Mitchell, J.; Milton, D. Aquametry : A Treatise on Methods for the Determination of Water, 2. ed.; Wiley: Hoboken, NJ, New York, , 1977.
[2]
Ooyama, Y.; Matsugasako, A.; Oka, K.; Nagano, T.; Sumomogi, M.; Komaguchi, K.; Imae, I.; Harima, Y. Chem. Commun. (Camb.), 2011, 47(15), 4448-4450.
[http://dx.doi.org/10.1039/c1cc10470e] [PMID: 21390355]
[3]
Ooyama, Y.; Sumomogi, M.; Nagano, T.; Kushimoto, K.; Komaguchi, K.; Imae, I.; Harima, Y. Org. Biomol. Chem., 2011, 9(5), 1314-1316.
[http://dx.doi.org/10.1039/C0OB00933D] [PMID: 21152608]
[4]
Ooyama, Y.; Matsugasako, A.; Hagiwara, Y.; Ohshita, J.; Harima, Y. RSC Advances, 2012, 2(20), 7666.
[http://dx.doi.org/10.1039/c2ra21067c]
[5]
Ooyama, Y.; Uenaka, K.; Matsugasako, A.; Harima, Y.; Ohshita, J. RSC Advances, 2013, 3(45), 23255.
[http://dx.doi.org/10.1039/c3ra42833h]
[6]
Ooyama, Y.; Furue, K.; Uenaka, K.; Ohshita, J. RSC Advances, 2014, 4(48), 25330.
[http://dx.doi.org/10.1039/c4ra02265c]
[7]
Citterio, D.; Minamihashi, T.K.; Kuniyoshi, Y.; Hisamoto, H.; Sasaki, S.; Suzuki, K. Anal. Chem., 2001, 73(21), 5339-5345.
[http://dx.doi.org/10.1021/ac010535q] [PMID: 11721939]
[8]
Niu, C.G.; Guan, A.L.; Zeng, G.M.; Liu, Y.G.; Li, Z.W. Anal. Chim. Acta, 2006, 577(2), 264-270.
[http://dx.doi.org/10.1016/j.aca.2006.06.046] [PMID: 17723682]
[9]
Niu, C.G.; Qin, P.Z.; Zeng, G.M.; Gui, X.Q.; Guan, A.L. Anal. Bioanal. Chem., 2007, 387(3), 1067-1074.
[http://dx.doi.org/10.1007/s00216-006-1016-y] [PMID: 17186226]
[10]
Niu, C.G. Anal. Sci., 2010, 26(6), 671-674.
[http://dx.doi.org/10.2116/analsci.26.671] [PMID: 20543498]
[11]
Li, Z.; Yang, Q.; Chang, R.; Ma, G.; Chen, M.; Zhang, W. Dyes Pigments, 2011, 88(3), 307-314.
[http://dx.doi.org/10.1016/j.dyepig.2010.07.009]
[12]
Liu, W.; Wang, Y.; Jin, W.; Shen, G.; Yu, R. Anal. Chim. Acta, 1999, 383(3), 299-307.
[http://dx.doi.org/10.1016/S0003-2670(98)00789-2]
[13]
Kim, J.S.; Choi, M.G.; Huh, Y.; Kim, M.H.; Kim, S.H.; Wang, S.Y.; Chang, S.K. Bull. Korean Chem. Soc., 2006, 27(12), 2058-2060.
[http://dx.doi.org/10.5012/bkcs.2006.27.12.2058]
[14]
Song, L.; Wu, Y-W.; Chai, W-X.; Tao, Y-S.; Jiang, C.; Wang, Q-H. Eur. J. Inorg. Chem., 2015, 2015(13), 2264-2271.
[http://dx.doi.org/10.1002/ejic.201500062]
[15]
Kim, Y.H.; Choi, M.G. Im, H. G.; Ahn, S.; Shim, I. W.; Chang, S. K. Dye. Pigment, 2012, 92, pp. (3)1199-1203.
[16]
Kim, Y-H.; Han, Y-K.; Kang, J. Bull. Korean Chem. Soc., 2011, 32(12), 4244-4246.
[http://dx.doi.org/10.5012/bkcs.2011.32.12.4244]
[17]
Moon, J-O.; Kim, Y-H.; Choi, M-G.; Chang, S-K. Bull. Korean Chem. Soc., 2011, 32(9), 3517-3520.
[http://dx.doi.org/10.5012/bkcs.2011.32.9.3517]
[18]
Myung, G.C.; Mi, H.K.; Hee, J.K.; Park, J.E.; Chang, S.K. Bull. Korean Chem. Soc., 2007, 28(10), 1818-1820.
[http://dx.doi.org/10.5012/bkcs.2007.28.10.1818]
[19]
Poteet, S.A.; MacDonnell, F.M. Dalton Trans., 2013, 42(37), 13305-13307.
[http://dx.doi.org/10.1039/c3dt51664d] [PMID: 23925310]
[20]
Men, G.; Zhang, G.; Liang, C.; Liu, H.; Yang, B.; Pan, Y.; Wang, Z.; Jiang, S. Analyst (Lond.), 2013, 138(10), 2847.
[http://dx.doi.org/10.1039/c3an36887d]
[21]
Pal, S.; Mukherjee, M.; Sen, B.; Lohar, S.; Chattopadhyay, P. RSC Advances, 2014, 4(41), 21608-21611.
[http://dx.doi.org/10.1039/C4RA02585G]
[22]
Cha, S.; Choi, M.G.; Jeon, H.R.; Chang, S-K. Sens. Actuators B Chem., 2011, 157(1), 14-18.
[http://dx.doi.org/10.1016/j.snb.2011.03.020]
[23]
Ma, W.; Jiang, S.; Zhang, W.; Xu, B.; Tian, W. Macromol. Rapid Commun., 2020, 20000032000003
[http://dx.doi.org/10.1002/marc.202000003]
[24]
Li, J.; Du, P.; Chen, J.; Huo, S.; Han, Z.; Deng, Y.; Chen, Y.; Lu, X. Anal. Chem., 2020, 92(13), 8974-8982.
[http://dx.doi.org/10.1021/acs.analchem.0c00966] [PMID: 32452666]
[25]
Zhang, K.; Chen, T-T.; Shen, Y-J.; Zhang, L-F.; Ma, S.; Huang, Y. Sens. Actuators B Chem., 2020, 311127887
[http://dx.doi.org/10.1016/j.snb.2020.127887]
[26]
Frisch, M. J.; Trucks, G. W.; Schlegel, H. B.; Scuseria, G. E.; Robb, M. A.; Cheeseman, J. R.; Scalmani, G.; Barone, V.; Petersson, G. A.; Nakatsuji, H.; Li, X.; Caricato, M.; Marenich, A.; Bloino, J.; Janesko, B. G.; Gomperts, R.; Mennucci, B.; Hratchian, H. P.; Ortiz, J. V.; Izmaylov, A. F.; Sonnenberg, J. L.; Williams-Young, D.; Ding, F.; Lipparini, F.; Egidi, F.; Goings, J.; Peng, B.; Petrone, A.; Henderson, T.; Ranasinghe, D.; Zakrzewski, V. G.; Gao, J.; Rega, N.; Zheng, G.; Liang, W.; Hada, M.; Ehara, M.; Toyota, K.; Fukuda, R.; Hasegawa, J.; Ishida, M.; Nakajima, T.; Honda, Y.; Kitao, O.; Nakai, H.; Vreven, T.; Throssell, K.; Montgomery, J. A., Jr; Peralta, J. E.; Ogliaro, F.; Bearpark, M.; Heyd, J. J.; Brothers, E.; Kudin, K. N.; Staroverov, V. N.; Keith, T.; Kobayashi, R.; Normand, J.; Raghavachari, K.; Rendell, A.; Burant, J. C.; Iyengar, S. S.; Tomasi, J.; Cossi, M.; Millam, J. M.; Klene, M.; Adamo, C.; Cammi, R.; Ochterski, J. W.; Martin, R. L.; Morokuma, K.; Farkas, O.; Foresman, J. B.; Fox, D. J. Gaussian 09 Revision A.02; Wallingford CTGaussian, Inc., 2016.
[27]
Jung, H.S.; Verwilst, P.; Kim, W.Y.; Kim, J.S. Chem. Soc. Rev., 2016, 45(5), 1242-1256.
[http://dx.doi.org/10.1039/C5CS00494B] [PMID: 26766615]
[28]
Contreras-García, J.; Johnson, E.R.; Keinan, S.; Chaudret, R.; Piquemal, J-P.; Beratan, D.N.; Yang, W. J. Chem. Theory Comput., 2011, 7(3), 625-632.
[http://dx.doi.org/10.1021/ct100641a] [PMID: 21516178]
[29]
Johnson, E.R.; Keinan, S.; Mori-Sánchez, P.; Contreras-García, J.; Cohen, A.J.; Yang, W. J. Am. Chem. Soc., 2010, 132(18), 6498-6506.
[http://dx.doi.org/10.1021/ja100936w] [PMID: 20394428]
[30]
Lu, T.; Chen, F. J. Comput. Chem., 2012, 33(5), 580-592.
[http://dx.doi.org/10.1002/jcc.22885] [PMID: 22162017]
[31]
Humphrey, W.; Dalke, A.; Schulten, K. J. Mol. Graph., 1996, 14(1), 33-38, 27-28.
[http://dx.doi.org/10.1016/0263-7855(96)00018-5] [PMID: 8744570]
[32]
Jeong, E.; Yoon, S.; Lee, H.S.; Kumar, A.; Chae, P.S. Dyes Pigments, 2019, 162, 348-357.
[http://dx.doi.org/10.1016/j.dyepig.2018.10.033]
[33]
Brouwer, A.M. Pure Appl. Chem., 2011, 83(12), 2213-2228.
[http://dx.doi.org/10.1351/PAC-REP-10-09-31]
[34]
Suzuki, K.; Kobayashi, A.; Kaneko, S.; Takehira, K.; Yoshihara, T.; Ishida, H.; Shiina, Y.; Oishi, S.; Tobita, S. Phys. Chem. Chem. Phys., 2009, 11(42), 9850-9860.
[http://dx.doi.org/10.1039/b912178a] [PMID: 19851565]
[35]
APEX3SAINT, and SADABS; Bruker AXS Inc.: Madison, WI, USA, 2018.
[36]
Sheldrick, G.M. Acta Crystallogr. A, 2008, 64(Pt 1), 112-122.
[http://dx.doi.org/10.1107/S0108767307043930] [PMID: 18156677]
[37]
Sheldrick, G.M. Acta Crystallogr. C Struct. Chem., 2015, 71(Pt 1), 3-8.
[http://dx.doi.org/10.1107/S2053229614024218] [PMID: 25567568]
[38]
Macrae, C.F.; Sovago, I.; Cottrell, S.J.; Galek, P.T.A.; McCabe, P.; Pidcock, E.; Platings, M.; Shields, G.P.; Stevens, J.S.; Towler, M. J. Appl. Cryst., 2020, 53(1), 226-235.
[http://dx.doi.org/10.1107/S1600576719014092]
[39]
Bandyopadhyay, P.; Ray, S.; Seikh, M.M. Phys. Chem. Chem. Phys., 2019, 21(48), 26580-26590.
[http://dx.doi.org/10.1039/C9CP05374C] [PMID: 31788678]
[40]
Desiraju, G.R. Acc. Chem. Res., 1991, 24(10), 290-296.
[http://dx.doi.org/10.1021/ar00010a002]
[41]
Desiraju, G.R. Acc. Chem. Res., 1996, 29(9), 441-449.
[http://dx.doi.org/10.1021/ar950135n] [PMID: 23618410]
[42]
Steiner, T. Crystallogr. Rev., 1996, 6(1), 1-51.
[http://dx.doi.org/10.1080/08893119608035394]
[43]
Steiner, T. Chem. Commun. (Camb.), 1997, 8, 727-734.
[http://dx.doi.org/10.1039/a603049a]
[44]
Desiraju, G.R.; Steiner, T. The Weak Hydrogen Bond in Structural Chemistry and Biology; Oxford University Press, 1999.
[45]
M. R., Luo, Ed.; Encyclopedia of Color Science and Technology; Springer New York: New York, NY, 2016.
[46]
Kumar, P.; Gadiyaram, S.; Jose, D.A. ChemistrySelect, 2020, 5, 10648-10655.
[http://dx.doi.org/10.1002/slct.202002530]

Rights & Permissions Print Cite
© 2024 Bentham Science Publishers | Privacy Policy