Topological Index of Conjugated Heterocyclic Compounds as Their Donor/Acceptor Parameter

References

• V. Sharma, P. Kumar, D. Pathak. “Biological Importance of the Indole Nucleus in Recent Years: A Comprehensive Review.” Journal of Heterocyclic Chemistry,” 47 (2010) 491–502.
   Web of Science ®Google Scholar
• A. Al-Mulla. “A Review: Biological Importance of Heterocyclic Compounds.” Der Pharma Chemica 9no. 13 (2017): 141–147. (http://www.derpharmachemica.com/archive.html)
   Google Scholar
• J. C. Crano, R. J. Guglielmetti. Organic Photochromic and Thermochromic Compounds. Volume 1: Main Photochromic Families Kluwer Academic Publishers. New York, Boston, Dordrecht, London, Moscow. (2002) 378P.
   Google Scholar
• S. Hünig, H. Berneth. “Two Step Reversible Redox Systems of the Weirz Type.” Topics Current Chemistry. In book: Organic Chemistry. 92 (1980) 1–44.
   Google Scholar
• J. M. Hales, S. Barlow, H. Kim, S. Mukhopadhyay, J.-L. Brédas, J. W. Perry, S. R. Marder. “ Design of Organic Chromophores for All-Optical Signal Processing Applications.” Chemistry of. Materials 26 (2014) 549−560.
   Web of Science ®Google Scholar
• L. G. S. Brooker. “ Spectra of Dye Molecules. Absorption and Resonance in Dyes.” Reviews of Modern Physics 14 (1942) 275–293.
   Google Scholar
• J. L. Bricks, A. D. Kachkovskii, Yu. L. Slominskii, A. O. Gerasov, S. V. Popov. “Molecular Design of Near Infrared Polymethine Dyes: A Review.” Dyes & Pigments. 121 (2015) 238–255. DOI: 10.1016/j.dyepig.2015.05.016.
   Web of Science ®Google Scholar
• A. V. Kulinich, A. A. Ishchenko. “Merocyanine Dyes: Synthesis, Structure, Properties and Applications.” Russian Chemical Reviews. 78 (2009) 141–164.
   Web of Science ®Google Scholar
• H. Mustroph, K. Reiner, B. Senns, J. Mistol, S. Ernst, D. Keil, L. Hennig. “The Effects of Substituents and Solvents on the Ground-State p-Electronic Structure and Electronic Absorption Spectra of a Series of Model Merocyanine Dyes and Their Theoretical Interpretation.” Chemistry A European Journal. 18 (2012) 8140–8149.
   PubMed Web of Science ®Google Scholar
• A. D. Kachkovsky. “The Nature of Electronic; Transitions in Linear Conjugated Systems.” Russian. Chemical Review 66 (8) (1997) 647 – 664. DOI: 10.1070/RC1997v066n08ABEH000274.
   Google Scholar
• W. Zaenger. Principles of Nucleic Acid Structure.New-York, Berlin, Heldelberg, Tokyo: Springer-Verlag. (1984) 584 p.
   Google Scholar
• G. R. Desiraju, T. Stainer. The Weak Hydrogen Bond on Structural Chemistry and Biology. New York: Oxford University Press Inc. (1999) 526 P. DOI: 10.1021/ja0047368.
   Google Scholar
• S. J. Grabowski “Hydrogen Bonding Strength. – Measures Based on Geometric and Topological Parameters.” Journal of Physical Organic Chemistry A. 105 (2001) 10739–10746.
   Web of Science ®Google Scholar
• N. Trinajstic. Hückel Theory and Topology. In: Segal G.A. (eds) Semiempirical Methods of Electronic Structure Calculation. Modern Theoretical Chemistry, vol 7. Boston, MA: Springer. (1977) 274P. DOI: 10.1007/978-1-4684-2556-7_1
   Google Scholar
• D. Bonchev, O. Mekenyan, N. Trinajstic. “ Topological Characterization of Cyclic Structures.” International Journal of. Quantum Chemistry. 17 (1980): 845–893.
   Web of Science ®Google Scholar
• D. Bonchev, O. Mekenyan, and O. E. Polansky. “A Topological Approach to the Predicting of the Electron Energy Characteristics of Conjugated Infinite Polymers. II. PPP– Calculations, Z. Naturforsch.,”. The Influence of Some Structural Modifications of Polymer, 36a, (1981): 643–646, 647–650.
   Google Scholar
• A. D. Kachkovsky, M.L. Dekhtyar. “Topological Indiced of Bicyclic End-group and Electronic Propertied of Linear Polymethine System.” Communications in mathematical and computer chemistry (Match). 32 (1995): 127–146.
   Google Scholar
• A. Streitwiser. Molecular Orbital Theory. (1963) 489P. New York, London: John Wiley and Sons, Inc.
   Google Scholar
• M. J. S. Dewar. The Molecular Orbital Theory of Organic Chemistry. (1969) 484P. New York: McGraw Hill.
   Google Scholar
• O. Shablykin, D. Merzhyievskyi, N. Obernikhina, O. Kobzar, Ya. Prostota, O. Kachkovsky, V. Brovarets, A. Vovk. Topological index of electronic structure of conjugated substituted bis-oxazoles and their spectral-luminescent properties//Conference Proceedings IEEE 38-th International Conference on Electronic and Nanotechnology (ELNANO-2018), (2018), 449-453.
   Google Scholar
• N. V. Pilipchuk, O.D. Kachkovski, D.A. Yushchenko, G.O. Kachkovski. “ Electronic Properties of Polymethine Systems 9: Position of Soliton Level in Charged Molecules.” Dyes and Pigments 66(3) (2005): 223–229.
   Web of Science ®Google Scholar
• M. J. Frisch, G. W. Trucks, H. B. Schlegel at all, (2009). GAUSSIAN09; revision B.05, Gaussian, Inc., Pittsburgh PA.
   Google Scholar
• A. Mishra, R. K. Behera, P. K. Behera, B. K. Mishra, G. B. Behera. “ Cyanine During the 1990s: A Review.” Chemical Reviews. 100 (2000): 1973–2011.
   PubMed Web of Science ®Google Scholar
• H. Hartmann, P. Gerstner, D. Rohde. “ A Simple Route to N-Arylated 2-Aminothiophenes as a New Class of Amorphous Glass Forming Molecules”. Organic Letters, 3 (11) (2001): 1673–1675. DOI: 10.1021/ol015875c.
   PubMed Web of Science ®Google Scholar
• R. S. H. Liu, A. E. Asato. “ Tuning the Color and Excited State Properties of the Azulenic Chromophore: NIR Absorbing Pigments and Materials.” Journal of Photochemistry and Photobiology C: Photochemistry. Reviews, 4 (2003): 179–194. DOI: 10.1016/j.jphotochemrev.2003.09.001.
   Web of Science ®Google Scholar
• J. Bricks, A. Ryabitskii, A. D. Kachkovski. “Studies of 2-Azaazulenium Derivatives: Different Types of Unsymmetrical Trimethine Cyanine Dyes Bearing 2-Azaazulenium Moiety as one of the Terminal Groups.” Chemistry, European Journal. 16(29). (2010): 8773–8784.
   PubMed Web of Science ®Google Scholar
• V. M. Orlov, A.N. Smirnov, Ya.M. Varshavsky. “ Ionization Potentials and Electron-donor Ability of Nucleic Acid Bases and Their Analogues.” Tetrahedron Letters. 48 (1976): 4377–4378.
   Web of Science ®Google Scholar
• E. C. M. Chen, E. S. D. Chen, N. Sane. “The Electron Affinities of the Radicals Formed by the Loss of an Aromatic Hydrogen Atom from Adenine, Guanine, Cytosine, Uracil, and Thymine.” Biochemical and biophysical research communications 246 (1998): 228–230.
   PubMed Web of Science ®Google Scholar