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Research Articles

Microwave-Assisted Synthesis, Physicochemical, and Optical Properties of Extended Pi (л) Bond Pyrazoline Derivative

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Pages 685-697 | Received 06 Nov 2018, Accepted 30 Apr 2019, Published online: 23 May 2019

References

  • S. Tarkuc, S. R. Eelkema, and F. C. Grozema, “The Relationship Between Molecular Structure and Electronic Properties in Dicyanovinyl Substituted Acceptor-Dono-Acceptor Chromophores,” Tetrahedron 73, (2017): 4994–5004.
  • X. B. Sun, Y. Q. Liu, X. J. Xu, C. H. Yang, G. Yu, S. Y. Chen, Z. H. Zhao, W. F. Qiu, Y. F. Li, and D. B. Zhu, “Novel Electroactive and Photoactive Molecular Materials Based on Conjugated Donor − Acceptor Structures for Optoelectronic Device Applications,” The Journal of Physical Chemistry B 109, no. 21 (2005): 10786–92.
  • L. Li, D. Liu, Z. Hong, S. Tong, P. Wang, C. Ma, O. Lengyel, C. S. Lee, H. L. Kwong, and S. Lee, “A New Family of Isophorone-Based Dopants for Red Organic Electroluminescent Devices,” Chemistry of Materials 15, no. 7 (2003): 1486–90.
  • J. Jayabharathi, E. Sarojpurani, V. Thanikachalam, and P. Jeeva, “Far-Field Enhancement by Silver Nanoparticles in Organic Light Emitting Diodes Based on Donor − π–Acceptor Chromophore,” Industrial & Engineering Chemistry Research 56, no. 18 (2017): 5325–38.
  • M. Ma, C. Ouyang, and H. Chen, “Design and Synthesis of Novel Chromophore with Multi-Carboxyl Groups,” Polycyclic Aromatic Compounds 38, no. 2 (2018): 103–9.
  • V. Hrobarikova, P. Hrobarik, P. Gajdos, I. Fitilis, M. Fakis, P. Persephonis, and P. Zahradnik, “Benzothiazole-Based Fluorophores of Donor − π-Acceptor − π-Donor Type Displaying High Two-Photon Absorption,” The Journal of Organic Chemistry 75, (2010): 3053–68.
  • S. Kumar, S. Bawa, S. Drabu, R. Kumar, and H. Gupta, “Biological Activities of Pyrazoline Derivatives—A Recent Development,” Recent Patents on Anti-Infective Drug Discovery 4, no. 3 (2009): 154–63.
  • A. Ahmad, A. Husain, S. A. Khan, M. Mujeeb, and A. Bhandari, “Synthesis, Antimicrobial and Antitubercular Activities of Some Novel Pyrazoline Derivatives,” Journal of Saudi Chemical Society 20, no. 5 (2016): 577–84.
  • C. K. Kumar, R. Trivedi, K. R. Kumar, L. Giribabu, and B. Sridhar, “Synthesis, Characterization, Electrochemistry and Optical Properties of New 1,3,5-Trisubstituted Ferrocenyl Pyrazolines and Pyrazoles Containing Sulfonamide Moiety,” Journal of Organometallic Chemistry 718, (2012): 64–73.
  • C. Chen, Y. Li, and L. Liu, “A High Quantum Yield Two-Way Conversion Luminescent Oligomer: 1,4-Butanediol-Bis(5-Carbonyl-3-Carbethoxy-2-Pyrazoline),” RSC Advances 6, no. 107 (2016): 105723–8.
  • Q. Peng, J. Zou, G. Zeng, Z. Wen, and W. Zheng, “Stable Blue-Emitting Molecular Material Derived from Calix[4]Arene Andpyrazoline Synthesis, Optical and Electrochemical Properties,” Synthetic Metals 159, no. 19–20 (2009): 1944–9.
  • J. Mysliwiec, A. Szukalski, L. Sznitko, A. Miniewicz, K. Haupa, K. Zygadlo, K. Matczyszyn, J. Olesiak-Banska, and M. Samoc, “Synthesis, Optical and Nonlinear Optical Properties of New Pyrazoline Derivatives,” Dyes and Pigments 102 (2014): 63–70.
  • Y. N. Singhbabu, P. Kumari, S. Parida, and R. K. Sahu, “Conversion of Pyrazolineto Pyrazole in Hydrazine Treated N-Substituted Reduced Graphene Oxide Films Obtained by Ion Bombardment and Their Electrical Properties,” Carbon 74, (2014): 32–43.
  • Z. Gong, L. Zheng, and B. Zhao, “Synthesis, X-Ray Crystal Structure and Optical Properties Research of Novel Diphenylsulfone-Based Bis-Pyrazoline Derivatives,” Journal of Luminescense 132 no. 2 (2012): 318–24.
  • C. Kumar, K. R. Trivedi, L. Giribabu, S. Niveditha, K. Bhanuprakash, and B. Sridhar, “Ferrocenylpyrazoline Based Multichannel Receptors for a Simple and Highly Selective Recognition of Hg2+ and Cu2+ Ions,” Journal of Organometallic Chemistry 780 (2015): 20–9.
  • V. Tirumalachetty, and K. Palaninathan, “Blue and Green Light Emitting Polyarylpyrazolinesluminogens Containing Anthracene and Thiophene Units,” Journal of Photochemistry and Photobiology A 359 (2018): 64–72.
  • B. Varghese, S. H. Al-Harthi, S. N. Al-Busafi, F. E. O. Suliman, S. M. Z. Al-Kindy andM, and T. Z. Myint, “Influence of Anchoring of a Pyrazoline Dye 3-Naphthyl-1-Phenyl-5 (4-Amino Phenyl)-2-Pyrazoline (NPAP) in Manipulating the Electronic and Chemical Properties of a Graphene Oxide via Amidation: Synthesis, Characterization and Photophysics,” Journal of Luminescense 192 (2017): 527–33.
  • E. Bozkurt, and H. I. Gul, “A Novel Pyrazoline-Based Fluorometric “Turn-off” Sensing for Hg2+,” Sensors and Actuators B: Chemistry 255 (2018): 814–25.
  • H. Jin, X. Li, T. Tan, S. Wang, Y. Xion, Y. Xino, and J. Thian, “Electrochromic Properties of Novel Chalcones Containing Triphenylamine Moiety,” Dyes and Pigments 106 (2014): 154–60.
  • S. Hu, S. Zhang, C. Gao, C. Xu, and Q. Gao, “A New Selective Fluorescent Sensor for Fe3+ Based on a Pyrazoline Derivative,” Spectrochimica Acta Part A 113 (2013): 325–31.
  • S. A. Khan, “Green Synthesis, Spectrofluorometric Characterization and Antibacterial Activity of Heterocyclic Compound from Chalcone on the Basis of in Vitro and Quantum Chemistry Calculation,” Journal of Fluorescence 27, no. 3 (2017): 929–37.
  • Y. Yang, S. Bo, H. Wang, F. Liu, J. Liu, L. Qiu, Z. Zhen, and X. Liu, “Novel Chromophores with Excellent Electro-Optic Activity Based on Double-Donor Chromophores by Optimizing Thiophene Bridges,” Dyes and Pigments 122, (2015): 139–46.
  • M. Jadhav, M. D. Patil, and N. Sekar, “Highly Stoke Shifted near Infrared (NIR) Emitting Donor-pi-Acceptor Chromophore: Synthesis and Combined Experimental and Computational Studies of Photophysical Properties,” Journal of Photochemistry and Photobiology A 363 (2018): 13–22.
  • G. J. Zhao, and K. L. Han, “Hydrogen Bonding in the Electronic Excited State,” Accounts of Chemical Research 45, no. 3 (2012): 404–13.
  • P. Suppan, “Invited Review Solvatochromic Shifts: The Influence of the Medium on the Energy of Electronic States,” Journal of Photochemistry and Photobiology A 50, no. 3 (1990): 293–330.
  • Y. Erande, S. Kothavale, M. C. Sreenath, S. Chitrambalam, I. H. Joe, and N. Sekar, “NLOphoricmultichromophoric Auxiliary Methoxy Aided Triphenylamine D-π-a Chromophores—Spectroscopic and Computational Studies,” Optical Materials 73 (2017): 602–16.
  • C. Zhang, L. Li, H. Wu, Z. Liu, J. Li, G. Zhang, G. Wen, S. Shuang, C. Dong, and M. M. F. Choi, “Synthesis and Photophysical Studies of Oxazole Rings Containing Compounds as Electron Accepting Units,” Spectrochim Acta A 102 (2013): 256–62.
  • G. Urut, O. D. Bayramin, and S. Alp, “Synthesis and Spectral Properties of New Ethylene Glycol Bridged Oxazol-5-Ones: High Stokes Shift Fluorophores Sensitive to Slovent Polarity,” Journal of Molecular Liquids 247 (2017): 109–15.
  • M. Aleksiejew, J. Heldt, and J. R. Heldt, “Experimental and Theoretical Spectroscopic Studies of Ortho Derivatives of Methyl p-Dimethylaminobenzoate,” Journal of Luminescense 129, no. 3 (2009): 208–20.
  • C. C. Chiu, W. C. Chen, and P. Y. Cheng, “Excited-State Vibrational Relaxation and Deactivation Dynamics of Trans-4-(N,N-Dimethylamino)-4′-Nitrostilbene in Nonpolar Solvents Studied by Ultrafast Time-Resolved Broadband Fluorescence Spectroscopy,” Journal of Photochemistry and Photobiology A 310 (2015): 26–32.
  • Y. Chen, B. Zhang, J.-G. Chen, and D.-Y. Huang, “Solvent Effects on the Absorption and Fluorescence Characteristics of Tin(IV) Mesoporphyrin,” Spectrochim Acta A 57, no. 12 (2001): 2451–6.
  • C. Reichardt, “Solvatochromic Dyes as Solvent Polarity Indicators,” Chemical Reviews 94, no. 8 (1994): 2319–58.
  • I. Thivaios, V. Koukoumtzis, J. K. Kallitsis, and G. Bokias, “Quinoline-Labeled Poly (N-Isopropylacrylamide): A Selective Polymeric Luminescent Sensor of Cationic Surfactants,” Sensors and Actuators B: Chemistry 233 (2016): 127–35.
  • S. A. Khan, A. M. Asiri, A. M. Al-Dies, O. I. Osman, M. Asad, and M. E. M. Zayed, “One-Pot Synthesis, Physicochemical and Photophysical Properties of Deep Blue Light-Emitting Highly Fluorescent Pyrene-Imidazole Dye: A Combined Experimental and Theoretical Studies,” Journal of Photochemistry and Photobiology A 364 (2018): 390–9.

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