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Studies on the charge density distribution in p-substituted phenylnitrenium cation

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PL
Badania nad rozkładem gęstości ładunku w p-podstawionym kationie fenylonitreniowym
Języki publikacji
EN
Abstrakty
EN
Aniline and its derivatives are known to be mutagenic. This activity is caused by the formation of phenylnitrenium cations during aniline oxidation. Reactivity of the positively charged chemical species can be measured by means of s+ substituent constant. In this paper charge density distribution in p-substituted nitrenium cations and reactivity indices such as, hardness η, electronegativity χ , and electrophilicily ω were analyzed. In order to evaluate which parameters are the most appropriate in describing electron density, correlation coefficients with s+ were calculated. The best results were achieved in case of energy of the lowest unoccupied molecular orbital (ELUMO). NBO lone pair orbital energy NBO ELP, and partial charge on the nitrenium nitrogen calculated using NBO method. NBO N charge. Analysis of these parameters showed that values of s+ depends strongly on the charge density on nitrenium nitrogen atom. According to NBO calculations. electron density on C-2 and C-6 (atoms numeration according to Fig. 1) is lower than in case of C-3 and C-5. These facts are consistent with the resonance theory.
PL
Anilina i jej pochodne wykazują właściwości mutageniczne. Ta aktywność wywołana jest powstawaniem kationu fenylonitreniowego podczas utleniania aniliny. W niniejszej publikacji, zbadana została dystrybucja gęstości ładunku w p-podstawionym kationie fenylonitreniowym. Przeanalizowano, wartości indeksów reaktywności, takich jak twardość η, elektroujemność χ, elektrofilowość ω oraz wartości ładunków Mullikena, NBO. CHelpG i APT. Aby stwierdzić które parametry są najlepsze do oceny gęstości elektronowej obliczono współczynniki korelacji dla tych parametrów z wartościami stałych podstawnika sp+. Najlepsze rezultaty uzyskano w przypadku energii poziomu LUMO, energii orbitaluwolnej pary elektronowej i ładunku NBO na nitreniowym atomie azotu. Analizy tych parametrów wykazały, że wartość stałej sp+ jest silnie uzależniona od gęstości ładunku na nitreniowym atomie azotu. Na podstawie obliczeń NBO stwierdzono, że gęstość elektronowa na atomach C-2 i C-6 jest mniejsza niż w przypadku C-3 i C-5. Przedstawione powyżej fakty są zgodne z teorią rezonansu.
Czasopismo
Rocznik
Strony
230--236
Opis fizyczny
Bibliogr. 36 poz., tab.
Twórcy
  • Nicolaus Copernicus University, Collegium Medicum.,Department of Physical Chemistry
Bibliografia
  • [1] Kim E.J., Matuszek A.M., Yu B., Reynisson J. 2011. Theoretical investigations into the role of aryl nitrenium ions. Stability on their mutagenic potential. Australian Journal of Chemistry 64: 910-915.
  • [2] McClelland R.A,. Postigo A. 2006. Solvent effects on the reactivity of fluorenyl nitrenium ion with DNA-like probes. Biophysical Chemistry 119: 213-218.
  • [3] Novak M., Kennedy S.A. 1998. Inhibitory effect of DNA structure on the efficiency of reaction of guanosine moieties with a nitreniumion. Journal of Physical Organic Chemistry 11: 71-76.
  • [4] Reynisson J., Stiborov M., Martínek V., da Costa G.G., Phillips D.H., Arlt V.M. 2008. Mutagenic potential of nitrenium ions of nitrobenzanthrones: Correlation between theory and experiment. Environmental and Molecular Mutagenesis 49: 659-667.
  • [5] Bentzien J., Hickey E.R., Kemper R.A., Brewer M.L.. Dyekjaer J.D., East S.P., Whittaker M. 2010. An in silico method for predicting Ames activities of primary aromatic amines by calculating the stabilities of nitrenium ions. Journal of Chemical Information and Modeling 50: 274-297.
  • [6] Marquez M., Mari F., Gonzalez C. A. 1999. Ab initio study of the reactions between a series of substituted singlet nitrenium ions and water Journal of Physical Chemistry A, 103: 6191-6199.
  • [7] Novak M., Rajagopal S. 2002. Correlations of nitrenium ion selectivilies with quantitative mutagenicity and carcinogenicity of the corresponding amines. Chemical Research in Toxicology. 15: 1495-1503.
  • [8] Bergeron R.J., Wiegand J., Bharti N., McManis J.S. 2012. Substituent effects on desferrithiocin and desferrithiocin analogue iron-clearing and toxicity profiles. Journal of Medical Chemistry 55: 7090- 103.
  • [9] Veith G.D., Mekenyan O.G., Ankley G.T., Call D.J. 1995. A QSAR analysis of substituent effects on the photoinduced acute toxicity of PAHs. Chemosphere. 30: 2129-214.
  • [10] Wright J.S. Shadnia H. 2008. Computational modeling of substituent effects on phenol toxicity, Chemical Research in Toxicology, 2: 1426-1431.
  • [11] Kuz’min V.E,. Muratov E.N., Artemenko A.G., Gorb L., Qasim M., Leszczyński J. 2008. The effects of characteristics of substituents on toxicity of the nitroaromatics: HiT QSAR study Journal of Computer-Aided Molecular Design. 22: 747-759.
  • [12] Hammett L.P. 1937. The effect of structure upon the reactions of organic compounds, benzene derivatives. Journal of the American Chemical Society. 59: 96-103.
  • [13] Mayr, H.: Palz, M. 1994. Scales of nucleophilicity and electrophilicity: A system for ordering polar organic and organometallic reactions. Angewandte Chemie International Edition in English. 33: 938-957.
  • [14] Mayr II.. Millier K.-H. Ofial A.R.. Buhl M. 1999. Comparison of the electrophilicities of the free and the (Tricarbonyl)iron-coordinated tropylium ion. Journal of the American Chemical Society. 121.2418-2424.
  • [15] Mayr H., Bug T., Gotta M.F., Hering N., Irgang B., Janker B., Kempf B., Loos R., Ofial A.R., Remennikov G., Schimmel H. 2001. Reference scales for the characterization of cationic electrophiles and neutral nucleophiles. Journal of the American Chemical Society, 123: 9500-9512.
  • [16] Mayr, H., Kempf, B., Ofial, A.R. 2003. ϖ -nucleophilicity in carbon-carbon bond forming reactions. Accounts of Chemical Research, 36: 66-77.
  • [17] Minegishi S., Mayr H. 2003. How constant are ritchie’s Constant selectivity relation- ships? A general reactivity scale for n-, ϖ- and σ-nucleophiles. Journal of the American Chemical Society. 125: 286-295.
  • [18] Minegishi S., Kobayashi S., Mayr H. 2004.,Solvent nucleophilicity. Journal of the American Chemical Society. 126: 5174-5181.
  • [19] Aizman A,. Contreras R., Perezc P. 2005. Relationship between local electrophilicity and,rate coefficients for the hydrolysis of carbenium ions. Tetrahedron, 61: 889-895.
  • [20] Hilala R., Khaleka A.A.A., Elrobyb S.A.K. 2005. DFT investigation of nitrenium ions derived from metabolizm of antitumor 2-(4-aminophenyl)benzothiazoles. Journal of Molecular Structure: Theochem, 731: 115-121.
  • [21] Frisch M.J., Trucks G.W., Schlegel H.B., Scuseria G.E.. Robb M.A., Cheeseman J.R., Montgomery J.A., Vreven T., Kudin K.N., Burant J.C., Millam J.M., Iyengar S.S., Tomasi J., Barone V., Mennucci B., Cossi M., Scalmani G., Rega N., Petersson G.A., Nakatsuji H., Hada M., Ehara M., Toyota K., Fukuda R., Hasegawa J., Ishida M,. NakajimaT., Honda Y., Kitao O., Nakai H., Kiene M., Li X., Knox J.E., Hratchian H.P., Cross J.B., Bakken V., Adamo C., Jaramillo J., Gomperts R., Stratmann R.E., Yazyev O., Austin A.J., Cammi R., Pomelli C., Ochterski J.W., Ayala P.Y., Morokuma K., Voth G.A., Salvador P., Dannenberg J.J., Zakrzewski V.G., Dapprich S., Daniels A.D., Strain. M.C., Farkas O., Malick D.K., Rabuck A.D., Raghavachari K., Foresman J.B., Ortiz J.V., Cui Q., Baboul A.G., Clifford S., Cioslowski J., Stefanov B.B., Liu G., Liashenko A., Piskorz P., Komaromi I., Martin R.L., Fox D.J., Keith T., Al-Laham M.A., Peng. C.Y., Nanayakkara A., Challacombe M., Gill P.M.W., Johnson B., Chen W., Wong M., Gonzalez W.C., Pople J.A., (2004) Gaussian 03 (Revision E. 01) Gaussian, Inc, Wallingford [Program komputerowy].
  • [22] Becke A.D. 1988. Density-functional exchange-energy approximation with correct asymptotic behavior. Physical Reviews A 38: 3098-3100.
  • [23] Becke A.D. 1993. Density-functional thermochemistry III. The role of exact exchange. Journal of Chemical Physics 98: 5648-5652.
  • [24] Lee C., Yang W., Parr R.G 1988, Development of the Colle-Salvetti correlation-energy formula into a functional of the electron density. Physical Review B 37: 785-789.
  • [25] Miertus S., Scrocco E., Tomasi J. 1981. Electrostatic interaction of a solute with a continuum. A direct utilization of ab initio molecular potentials for the prevision of solvent effects. Chemical Physics, 55: 117-129.
  • [26] Miertuš S., Tomasi J. 1982. Approximate evaluations of the electrostatic free energy and internal energy changes in solution processes. Chemical Physics, 65: 239-241.
  • [27] Pearson R.G. 1986. Proceedings of the National Academy of Science of the USA, 83: 8440-8441.
  • [28] Parr R.G., von Szentpály L., Liu S. 1999. Electrophilicity index. Journal of the American Chemical Society. 121: 1922 1924.
  • [29] Kruszewski J., Krygowski T.M. 1972. Harmonical oscillator approach to the definition of aromaticity. Tetrahedron letters, 13: 3839-3842.
  • [30] Krygowski T.M., Cyrahski M.K., Czarnocki Z., Haäfelinger G., Katritzky A.R. 2000. Aromaticity: a theoretical concept of immense practical importance. Tetrahedron. 56: 1783- 1796.
  • [31] Mulliken R.S. 1955. Electronic population analysis on LCAO-MO molecular wave functions. I. The Journal of Chemical Physics 23: 1833-1840.
  • [32] Foster J.P., Weinhold F. 1980. Natural hybrid orbitals. Journal of the American Chemical Society. 102: 7211-7218.
  • [33] Cioslowski J. 1989. A new population analysis based on atomic polar tensors. Journal of the American Chemical Society. Ill: 8333-8336.
  • [34] Kollman S.P.A. 1984. An approach to computing electrostatic charges for molecules. Journal of Computational Chemistry 5: 129-145.
  • [35] Hansch C., Leo A., Taft R.W. 1991. A survey of Hammett substituent constants and resonance and field parameters. Chemical Reviews 91: 165-195.
  • [36] Sullivan M.B., Brown K., Cramer C.J., Truhlar D.G. 1998. Journal of the American Chemical Society, Quantum Chemical Analysis of para-Substitution Effects on the Electronic Structure of Phenvlnitrenium Ions in the Gas Phase and Aqueous Solution 120: 11778-11783.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-37128e13-1137-4830-8ab7-cd942801ca74
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