[1] R.S. Mulliken, Molecular compounds and their spectra. II, J. Am. Chem. Soc., 74 (1952) 811-824.
https://doi.org/10.1021/ja01123a067
[2] J.N. Murrell, The theory of charge-transfer spectra, Quarterly Rev. Chem. Soc., 15 (1961) 191-206.
https://doi.org/10.1039/QR9611500191
[3] J. Weiss, The formation and structure of some organic molecular compounds, J. Chem. Soc., (1942) 245-252.
https://doi.org/10.1039/JR9420000245
[4] H. Miyasaka, Control of charge transfer in donor/acceptor metal–organic frameworks, Accounts Chem. Res., 46 (2013) 248-257.
https://doi.org/10.1021/ar300102t
[5] Y. Kato, H. Matsumoto, T. Mori, Absence of HOMO/LUMO transition in charge-transfer complexes of thienoacenes, J. Phys. Chem., A 125 (2021) 146-153.
https://doi.org/10.1021/acs.jpca.0c08925
[6] G.R. Anderson, Symmetry classification and selection rules for some electron donor-acceptor complexes, J. Am. Chem. Soc., 92 (1970) 3552-3560.
https://doi.org/10.1021/ja00715a005
[7] D. Booth, Charge-transfer molecular complexes and their role in chemical reactions, Sci. Progress, 48(1960) 435-455.
https://www.jstor.org/stable/43417573
[8] A. Müllertz, T. Rades, Evaluating oral drug delivery systems: dissolution models, Springer Publisher, Anal. Tech. Pharm. Sci., (2016) 753-771.
https://doi.org/10.1007/978-1-4939-4029-5
[9] C. Arrell, L. Longetti, M. Chergui, J. Helbing, Charge-transfer and impulsive electronic-to-vibrational energy conversion in ferricyanide: Ultrafast photoelectron and transient infrared studies, Phys. Chem. Chem. Phys., 19 (2017) 17052-17062.
https://doi.org/10.1039/C7CP03337K
[10] S. S. Swayamprabha, D. K. Dubey, Shahnawaz, R.A.K. Yadav, M.R. Nagar, A. Sharma, F. Tung, J. Jou, Approaches for long lifetime organic light emitting diodes, Adv. Sci. 8 (2021) 2002254.
https://doi.org/10.1002/advs.202002254
[11] H.J. Kim, T. Yasuda, Narrowband emissive thermally activated delayed fluorescence materials, Adv. Optic. Mater., 10 (2022) 2201714.
https://doi.org/10.1002/adom.202201714
[12] A. Hillier, G. Mao, Charge‐transfer complexes: Fundamentals and advances in catalysis, Sensing, and optoelectronic applications, Adv. Mater., 36 (2024) 2406083.
https://doi.org/10.1002/adma.202406083
[13] M. Cai, C. Shang, F. Bi, F. Feng, Z. Du, C. Sun, Y. Li, X. Bao, Regulating intramolecular charge transfer and resonance effects to realize ultrawide bandgap conjugated polymer for high‐performance all‐Polymer solar cells, Adv. Funct. Mater., 33 (2023) 2301701.
https://doi.org/10.1002/adfm.202301701
[14] M. Waqas, Z. Aloui, M. Essid, M. Ibrahim, R. Khera, M. Shaban, M. Ans, Exploring the electronic, optical, and charge transfer properties of ADA-type IDTV-ThIC-based molecules to enhance photovoltaic performance of organic solar cells, ACS Omega, 8 (2023) 45384-45404.
https://doi.org/10.1021/acsomega.3c04437
[15] L. Liu, S. Zhao, S. Yang, D. Si, Q. Wu, Q. Wu, Y. Huang, R. Cao, Rapid charge transfer in covalent organic framework via through-bond for enhanced photocatalytic CO
2 reduction, Chem. Eng. J., 458 (2023) 141360.
https://doi.org/10.1016/j.cej.2023.141360
[16] W. Jung, S. Gonzalez-Carrero, J. Durrant, H. Cha, T. Park, Understanding charge carrier dynamics in organic photocatalysts for hydrogen evolution, Energ. Environ. Sci., 17(2024) 7999-8018.
https://doi.org/10.1039/D4EE01808G
[17] Liu, L. Fu, J. Liu, M. Wang, J. Zhou, Structure regulation of 2D materials by atom confinement for electrocatalysis, Coord. Chem. Rev., 520 (2024) 216164.
https://doi.org/10.1016/j.ccr.2024.216164
[18] S. Mal, S. Bhattacharyya, Deciphering interfacial charge transfer mechanisms in electrochemical energy systems through impedance spectroscopy, J. Mater. Chem. A, 12 (2024)14334-14353.
https://doi.org/10.1039/D4TA00537F
[19] M. Islam, S. K. Mustafa, A. Alessa, M. Al Ahjohani, N. Omer, R. Jame, I. Alatawi, M. Sagheer, Analysis the formation of H-bonded charge transfer complex of M-nitroaniline with oxalic acid in ethanol: Investigation its antimicrobial studies, DNA binding and molecular docking, DNA binding and molecular docking, Available at SSRN 4791207.
https://dx.doi.org/10.2139/ssrn.4791207
[20] M.S. Refat, A.M. Alsuhaibani, M. Islam, Biological and computational exploration of a hydrogen-bonded charge transfer complex between 8-Hydroxyquinoline and Benzene-1, 4-diol in different polar solvents: synthesis and spectrophotometric analysis, Available at SSRN 4847578.
https://dx.doi.org/10.2139/ssrn.4847578
[21] N. Alam, M. Islam, H. Najnin, S. Shakya, I. Khan, M. Hossain, R. Zaidi, Design and characterization of a binary CT complex of imidazole-oxyresveratrol: exploring its pharmacological and computational aspects, J. Biomol. Struct. Dyn., 42 (2024) 1319-1335.
https://doi.org/10.1080/07391102.2023.2199088
[22] A. Radwan, N. Alzoman, I. Darwish, Formation and characterization of charge transfer complex between alectinib and 2, 3-dichloro-5, 6-dicyano-1, 4-benzoquinone: Application to development of microwell spectrophotometric method, Sustain. Chem. Pharm., 39 (2024) 101524.
https://doi.org/10.1016/j.scp.2024.101524
[23] A. Nies, Minoxidil, Ann. Intern. Med., 94 (1981) 61-65.
https://www.acpjournals.org/doi/abs/10.7326/0003-4819-94-1-61
[24] N. Farjo, S. Picksley, V. Randall, Human hair follicles contain two forms of ATP‐sensitive potassium channels, only one of which is sensitive to minoxidil, FASEB Journal 22 (2008)1725-1736.
https://doi.org/10.1096/fj.07-099424
[25] G.R. Zins, The history of the development of minoxidil, Clin. Dermatol., 6 (1988) 132-147.
https://doi.org/10.1016/0738-081X(88)90078-8
[26] M. Talukder, G. Williams, Comparison of oral minoxidil, finasteride, and dutasteride for treating androgenetic alopecia, J. Dermatol. Treat., 33 (2022) 2946-2962.
https://doi.org/10.1080/09546634.2022.2109567
[27] M.G. Fraile, Theoretical characterization of new dynamic bonds for responsive materials and their optical properties, Diss. Universidad del País Vasco-Euskal Herriko Unibertsitatea, 2023.
https://dialnet.unirioja.es/servlet/tesis?codigo=322971
[28] Y. Tang, G. Han, Recent advances in the synthesis of aromatic azo compounds, Molecules, 28 (2023) 6741.
https://doi.org/10.3390/molecules28186741
[29] I. Mushtaq, M. Ahmad, M. Saleem, A. Ahmed, Pharmaceutical significance of Schiff bases: An overview, Futur. J. Pharm. Sci., 10 (2024) 16.
https://doi.org/10.1186/s43094-024-00594-5
[30] L. Ahamed, S. AL-Khazraji, Synthesis, characterization, and study of anticancer activities of new Schiff bases and 1, 3-oxazepine containing drug, Russ. J. Bioorg. Chem., 50 (2024) 28-33.
https://doi.org/10.1134/S1068162024010102
[31] H. Nassar, M. Abou-El-Wafa, H. Elkik, Synthesis and characterization of some coordinated metal and charge transfer complexes of isonicotinic acid hydrazide ligand with 2-hydroxyacetophenonylidene, Spectrochim. Acta A: Mol. Biomol. Spectrosc., 309 (2024) 123759.
https://doi.org/10.1016/j.saa.2023.123759
[32] M. Ayaz, A. Alam, Zainab, A. Elhenawy, N. Rehman, S. Rahman, M. Ali, Abdul Latif, A. Al-Harrasi, M. Ahmad, Designing and synthesis of novel fexofenadine‐derived hydrazone‐Schiff bases as potential urease inhibitors: In‐vitro, molecular docking and DFT investigations, Chem. Biodivers., 21 (2024) e202400704.
https://doi.org/10.1002/cbdv.202400704
[33] F. Dai, Q. Zhuang, G. Huang, H. Deng, X. Zhang, Infrared spectrum characteristics and quantification of OH groups in coal, ACS Omega, 8 (2023) 17064-17076.
https://doi.org/10.1021/acsomega.3c01336
[34] L.A. Mohammed, R. T. Mehdi, A. A. Mohammed Ali, Synthesis and biological screening of the gold complex as anticancer and some transition metal complexes with new heterocyclic ligand derived from 4-Amino Antipyrine, Nano Biomed., 10 (2018) 199-212.
https://doi.org/10.5101/nbe.v10i3.p199-212
[35] S. O. Aljazzar, Composition and decomposition of several Schiff base metal complexes containing Co (II) and Ni (II) ions: Spectroscopic analysis, Mor. J. Chem., 12 (2024) 180-198.
https://doi.org/10.48317/IMIST.PRSM/morjchem-v12i1.43061
[36] F. Naaz, S. Shakya, M. Islam, A. Khan, M. Ahmad, Photocatalytic activity, DFT/TD-DFT, and spectrophotometric studies of a synthesized charge transfer complex of p-toluidine with 1, 2, 4, 5-benzenetetracarboxylic acid in various polar solvents, J. Mol. Liq., 399 (2024) 124412.
https://doi.org/10.1016/j.molliq.2024.124412
[37] D. Ivanov, Y. Yang, Mass spectrometry‐based methods to characterize highly heterogeneous biopharmaceuticals, vaccines, and nonbiological complex drugs at the intact‐mass level, Mass Spect. Rev., 43 (2024) 139-165.
https://doi.org/10.1002/mas.21829
[38] S. Munusamy, M. Saravanakumar, M. Sekar, K. Muthusamy, M. Kumar, G. Vinitha, Exploring the structural and optical characteristics of the charge transfer complex 2, 3-dimethylquinoxaliniumpicrate: a comprehensive investigation through experimental and computational approaches, J. Mater. Sci.: Mater. Electron., 35 (2024) 1314.
https://doi.org/10.1007/s10854-024-12989-4
[39] N. Alalam, S. Bashir, Analytical applications of some N, NBPAD Schiff’s base for spectrophotometric determination of Chromium (VI), Chem. Res. J., 9 (2024): 86-93.
https://doi.org/10.5281/zenodo.11275451
[40] M. Al Mufty, M. Hailat, R. Awad, M. Awad, M. Hamad, Development and validation of a method for analyzing the combination of etoricoxib and acetaminophen in tablet dosage form, J. Hunan Univ. Nat. Sci., 51 (2024) 1-13.
https://doi.org/10.55463/issn.1674-2974.51.5.1
[41] A. Amin, A. Gouda, R. Sharaf, A. Elkhashab, G. Elasala, Validated spectrophotometric methods for determination of selegiline HCl as an irreversible inhibitor of monoamine oxidase in pure form and pharmaceutical formulations, TWIST Int. Multidiscip. J., 19 (2024) 176-186.
https://twistjournal.net/twist/article/view/156
[42] Sh. Teimoori, H. Shirkhanloo, A. Hassani, M. Panahi, N. Mansouri, Toxicological profile for ethylbenzene, benzene and xylene, Food Chem, 421 (2023) 136229.
https://doi.org/10.1016/j.foodchem.2023.136229
[43] J. Rakhtshah, H. Shirkhanloo, N. Esmaeil, A rapid extraction of toxic styrene from water and wastewater samples based on hydroxyethyl methylimidazolium tetrafluoroborate immobilized on MWCNTs by ultra-assisted dispersive cyclic conjugation-micro-solid phase extraction Author links open overlay panel, Microchem. J., 170 (2021) 106759. https://doi.org/10.1016/j.microc.2021.106759
[44] S. Teimoori, A. H. Hassani, M. Panahi, N. Mansouri, An immobilization of aminopropyl trimethoxysilane-phenanthrene carbaldehyde on graphene oxide for toluene extraction and separation in water samples, Chemosphere, 316 (2023) 137800. https://doi.org/10.1016/j.chemosphere.2023.137800
[45] S. Teimoori, A. H. Hassani, M. Panahi, N. Mansouri, Rapid extraction of BTEX in water and milk samples based on functionalized MWCNTs by dispersive homogenized-micro-solid phase extraction, Food Chem., 421 (2023) 136229. https://doi.org/10.1016/j.foodchem.2023.136229
[46] A.M. Ali, M. Abdulzahra, M. Abdali, Spectrophotometric determination of gancyclovir drug by combination reaction with NQS as a reagent, AIP Conf. Proc., 3092 (2024) 030007.
https://doi.org/10.1063/5.0199700