메뉴 건너뛰기




Volumn 106, Issue 6, 2006, Pages 2065-2091

Electrophilicity index

Author keywords

[No Author keywords available]

Indexed keywords

ELECTRON ENERGY LEVELS; ELECTRONIC DENSITY OF STATES; ELECTRONIC STRUCTURE; ELECTRONS; EXCITONS; GROUND STATE; PROBABILITY DENSITY FUNCTION;

EID: 33745756260     PISSN: 00092665     EISSN: None     Source Type: Journal    
DOI: 10.1021/cr040109f     Document Type: Review
Times cited : (1559)

References (440)
  • 16
    • 0003438540 scopus 로고
    • 3rd ed.; Cornell University Press: Ithaca, New York
    • Pauling, L. The Nature of the Chemical Bond, 3rd ed.; Cornell University Press: Ithaca, New York, 1960.
    • (1960) The Nature of the Chemical Bond
    • Pauling, L.1
  • 23
    • 0039003519 scopus 로고
    • Density Functional Theory of Chemical Hardness
    • Sen, K. D., Mingos, D. M. P., Eds.; Springer-Verlag: Berlin
    • Chattaraj, P. K.; Parr, R. G. Density Functional Theory of Chemical Hardness. In Chemical Hardness, Structure and Bonding; Sen, K. D., Mingos, D. M. P., Eds.; Springer-Verlag: Berlin, 1993; Vol. 80, pp 11-25.
    • (1993) Chemical Hardness, Structure and Bonding , vol.80 , pp. 11-25
    • Chattaraj, P.K.1    Parr, R.G.2
  • 25
    • 4644369879 scopus 로고    scopus 로고
    • Reactivity Descriptors
    • Tollenaere, J., Bultinck, P., Winter, H. D., Langenaeker, W., Eds.; Marcel Dekker: New York, Chapter 11
    • Chattaraj, P. K.; Nath, S.; Maiti, B. Reactivity Descriptors. In Computational Medicinal Chemistry for Drug Discovery; Tollenaere, J., Bultinck, P., Winter, H. D., Langenaeker, W., Eds.; Marcel Dekker: New York, 2003; Chapter 11, pp 295-322.
    • (2003) Computational Medicinal Chemistry for Drug Discovery , pp. 295-322
    • Chattaraj, P.K.1    Nath, S.2    Maiti, B.3
  • 27
    • 33745737595 scopus 로고    scopus 로고
    • [See also the Special Issue of Guest Editor: Chattaraj, P. K
    • [See also the Special Issue of J. Chem. Sci. on Chemical Reactivity, 2005, Vol. 117, Guest Editor: Chattaraj, P. K.
    • (2005) J. Chem. Sci. on Chemical Reactivity , vol.117
  • 28
    • 27844509495 scopus 로고    scopus 로고
    • There are several related papers in this issue, which include the following
    • There are several related papers in this issue, which include the following: Melin, J.; Ayers, P. W.; Ortiz, J. V. J. Chem. Sci. 2005, 117, 387.
    • (2005) J. Chem. Sci. , vol.117 , pp. 387
    • Melin, J.1    Ayers, P.W.2    Ortiz, J.V.3
  • 43
  • 49
    • 0011697104 scopus 로고    scopus 로고
    • [See to see the external potential effects on this principle.]
    • [See Cedillo, A.; Chattaraj, P. K.; Parr, R. G. Int. J. Quantum Chem. 2000, 77, 403 to see the external potential effects on this principle.]
    • (2000) Int. J. Quantum Chem. , vol.77 , pp. 403
    • Cedillo, A.1    Chattaraj, P.K.2    Parr, R.G.3
  • 51
    • 24644452555 scopus 로고    scopus 로고
    • [See for a connection between MHP and HSABP.] Note that the arithmetic mean principle for softness and MHP together imply HSABP
    • [See Chattaraj, P. K.; Ayers, P. W. J. Chem. Phys. 2005, 123, 086101 for a connection between MHP and HSABP.] Note that the arithmetic mean principle for softness and MHP together imply HSABP.
    • (2005) J. Chem. Phys. , vol.123 , pp. 086101
    • Chattaraj, P.K.1    Ayers, P.W.2
  • 53
    • 33745752777 scopus 로고
    • See refs 36 and 38 for a connection between MHP and HSABP
    • Chattaraj, P. K.; Nath, S. Ind. J. Chem. A 1994, 33A, 842. See refs 36 and 38 for a connection between MHP and HSABP.
    • (1994) Ind. J. Chem. A , vol.33 A , pp. 842
    • Chattaraj, P.K.1    Nath, S.2
  • 81
    • 0346948866 scopus 로고
    • Fukui, K. Science 1982, 218, 747.
    • (1982) Science , vol.218 , pp. 747
    • Fukui, K.1
  • 123
    • 33645705342 scopus 로고    scopus 로고
    • Although it was claimed in this paper that the local electrophilicity is a more reliable descriptor than its global counterpart, in two recent publications
    • Although it was claimed in this paper that the local electrophilicity is a more reliable descriptor than its global counterpart, in two recent publications [Roy, R. K.; Usha, V.; Patel, B. K.; Hirao, K. J. Comput. Chem. 2006, 27, 773.
    • (2006) J. Comput. Chem. , vol.27 , pp. 773
    • Roy, R.K.1    Usha, V.2    Patel, B.K.3    Hirao, K.4
  • 124
    • 33644760763 scopus 로고    scopus 로고
    • based on the numerical calculation on a different set of molecules, the authors have prescribed just the opposite. Where both fail, other factors such as steric effects are mentioned to be the plausible reasons. We feel that both global and local descriptors, other charge-based descriptors, and, if possible, other effects, such as steric, solvent, and entropy effects, are to be considered in order to have better insights into the chemical reactivity and selectivity. Of course, a few of them will dominate over the rest and some will be dependent on the others. We hope that it would be possible to identify the appropriate descriptor(s) for a given class of molecules/reactions prior to the computation and not after comparing the numerical results with the corresponding experimental trends
    • Roy, R. K.; Bagaria, P.; Naik, S.; Kavala, V.; Patel, B. K. J. Phys. Chem. A 2006, 110, 2181.] based on the numerical calculation on a different set of molecules, the authors have prescribed just the opposite. Where both fail, other factors such as steric effects are mentioned to be the plausible reasons. We feel that both global and local descriptors, other charge-based descriptors, and, if possible, other effects, such as steric, solvent, and entropy effects, are to be considered in order to have better insights into the chemical reactivity and selectivity. Of course, a few of them will dominate over the rest and some will be dependent on the others. We hope that it would be possible to identify the appropriate descriptor(s) for a given class of molecules/reactions prior to the computation and not after comparing the numerical results with the corresponding experimental trends.
    • (2006) J. Phys. Chem. A , vol.110 , pp. 2181
    • Roy, R.K.1    Bagaria, P.2    Naik, S.3    Kavala, V.4    Patel, B.K.5
  • 225
    • 33745741412 scopus 로고    scopus 로고
    • arXiv:cond-mat/0511441. Note that Δω is a better intermolecular descriptor than Δf because of the global information in the former. A portion of this work was presented at the 231st annual meeting of the American Chemical Society in Atlanta, GA
    • (b) Roy, D. R.; Subramanian, V.; Chattaraj, P. K. Los Alamos Natl. Lab., Prepr. Arch., Condsens. Matter 2005, 1-21, arXiv:cond-mat/0511441. Note that Δω is a better intermolecular descriptor than Δf because of the global information in the former. A portion of this work was presented at the 231st annual meeting of the American Chemical Society in Atlanta, GA.
    • (2005) Los Alamos Natl. Lab., Prepr. Arch., Condsens. Matter , pp. 1-21
    • Roy, D.R.1    Subramanian, V.2    Chattaraj, P.K.3
  • 243
    • 77952365810 scopus 로고    scopus 로고
    • Dutta, R. L., Ed.; The New Book Stall: Kolkata
    • (b) Inorganic Chemistry, Part-I Principles; Dutta, R. L., Ed.; The New Book Stall: Kolkata, 2003.
    • (2003) Inorganic Chemistry, Part-I Principles
  • 255
    • 0000947119 scopus 로고    scopus 로고
    • Ayers, P.W. Private communication. Excited-state reactivity may be analyzed through Levy - Nagy
    • Ayers, P. W. Private communication. Excited-state reactivity may be analyzed through Levy - Nagy [Levy, M.; Nagy, A. Phys. Rev. Lett. 1999, 83, 4361]
    • (1999) Phys. Rev. Lett. , vol.83 , pp. 4361
    • Levy, M.1    Nagy, A.2
  • 256
    • 0001102132 scopus 로고
    • or Görling functionals
    • or Görling [Görling, A. Phys. Rev. A 1993, 47, 2783] functionals.
    • (1993) Phys. Rev. A , vol.47 , pp. 2783
    • Görling1
  • 356
    • 0002078362 scopus 로고    scopus 로고
    • Tapia, O., Bertrán, J., Eds.; Kluwer Academic Publishers: Dordrecht, The Netherlands
    • Contreras, R.; Pérez, P.; Aizman, A. In Solvent Effects and Chemical Reactivity; Tapia, O., Bertrán, J., Eds.; Kluwer Academic Publishers: Dordrecht, The Netherlands, 1996; Vol. 17, p 81.
    • (1996) Solvent Effects and Chemical Reactivity , vol.17 , pp. 81
    • Contreras, R.1    Pérez, P.2    Aizman, A.3
  • 371
    • 0003078007 scopus 로고
    • Ultimate Chemical Carcinogens as Reactive Mutagenic Electrophiles
    • Hiatt, H. H., Watson, J. D., Winsten, J. A., Eds.; Cold Spring Harbor Laboratory Press: Cold Spring Harbor, NY
    • Miller, J. A.; Miller, E. C. Ultimate Chemical Carcinogens as Reactive Mutagenic Electrophiles. In Origins of Human Cancer; Hiatt, H. H., Watson, J. D., Winsten, J. A., Eds.; Cold Spring Harbor Laboratory Press: Cold Spring Harbor, NY, 1977; pp 605-627.
    • (1977) Origins of Human Cancer , pp. 605-627
    • Miller, J.A.1    Miller, E.C.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.