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Pregled bibliografske jedinice broj: 246502

Kinetics of the Solvolyses of Benzhydryl Derivatives: Basis for the Construction of a Comprehensive Nucleofugality Scale


Denegri, Bernard; Andre, Streiter; Ofial, Armin; Jurić, Sandra; Kronja, Olga; Mayr, Herbert
Kinetics of the Solvolyses of Benzhydryl Derivatives: Basis for the Construction of a Comprehensive Nucleofugality Scale // Chemistry : a European journal, 12 (2006), 6; 1648-1656 doi:10.1002/chem.200500845 (međunarodna recenzija, članak, znanstveni)


CROSBI ID: 246502 Za ispravke kontaktirajte CROSBI podršku putem web obrasca

Naslov
Kinetics of the Solvolyses of Benzhydryl Derivatives: Basis for the Construction of a Comprehensive Nucleofugality Scale

Autori
Denegri, Bernard ; Andre, Streiter ; Ofial, Armin ; Jurić, Sandra ; Kronja, Olga ; Mayr, Herbert

Izvornik
Chemistry : a European journal (0947-6539) 12 (2006), 6; 1648-1656

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni

Ključne riječi
carbocations • kinetics • nucleophilic substitution • reaction mechanisms • solvent effects

Sažetak
A series of 21 benzhydrylium ions (diarylmethylium ions) are proposed as reference electrofuges for the development of a general nucleofugality scale, where nucleofugality refers to a combination of leaving group and solvent. A total of 167 solvolysis rate constants of benzhydrylium tosylates, bromides, chlorides, trifluoroacetates, 3, 5-dinitrobenzoates, and 4-nitrobenzoates, two-thirds of which have been determined during this work, were subjected to a least-squares fit according to the correlation equation log k25 °C = sf(Nf + Ef), where sf and Nf are nucleofuge-specific parameters and Ef is an electrofuge-specific parameter. Although nucleofuges and electrofuges characterized in this way cover more than 12 orders of magnitude, a single set of the parameters, namely sf, Nf, and Ef, is sufficient to calculate the solvolysis rate constants at 25 °C with an accuracy of ± ; ; 16 %. Because sf1 for all nucleofuges, that is, leaving group/solvent combinations, studied so far, qualitative discussions of nucleofugality can be based on Nf.

Izvorni jezik
Engleski

Znanstvena područja
Kemija

Napomena
Ispravak u: 12 (2006) (21) str.5415.



POVEZANOST RADA


Projekti:
0006451

Ustanove:
Farmaceutsko-biokemijski fakultet, Zagreb

Profili:

Avatar Url Bernard Denegri (autor)

Avatar Url Olga Kronja (autor)

Avatar Url Sandra Jurić (autor)

Poveznice na cjeloviti tekst rada:

doi onlinelibrary.wiley.com

Citiraj ovu publikaciju:

Denegri, Bernard; Andre, Streiter; Ofial, Armin; Jurić, Sandra; Kronja, Olga; Mayr, Herbert
Kinetics of the Solvolyses of Benzhydryl Derivatives: Basis for the Construction of a Comprehensive Nucleofugality Scale // Chemistry : a European journal, 12 (2006), 6; 1648-1656 doi:10.1002/chem.200500845 (međunarodna recenzija, članak, znanstveni)
Denegri, B., Andre, S., Ofial, A., Jurić, S., Kronja, O. & Mayr, H. (2006) Kinetics of the Solvolyses of Benzhydryl Derivatives: Basis for the Construction of a Comprehensive Nucleofugality Scale. Chemistry : a European journal, 12 (6), 1648-1656 doi:10.1002/chem.200500845.
@article{article, author = {Denegri, Bernard and Andre, Streiter and Ofial, Armin and Juri\'{c}, Sandra and Kronja, Olga and Mayr, Herbert}, year = {2006}, pages = {1648-1656}, DOI = {10.1002/chem.200500845}, keywords = {carbocations • kinetics • nucleophilic substitution • reaction mechanisms • solvent effects}, journal = {Chemistry : a European journal}, doi = {10.1002/chem.200500845}, volume = {12}, number = {6}, issn = {0947-6539}, title = {Kinetics of the Solvolyses of Benzhydryl Derivatives: Basis for the Construction of a Comprehensive Nucleofugality Scale}, keyword = {carbocations • kinetics • nucleophilic substitution • reaction mechanisms • solvent effects} }
@article{article, author = {Denegri, Bernard and Andre, Streiter and Ofial, Armin and Juri\'{c}, Sandra and Kronja, Olga and Mayr, Herbert}, year = {2006}, pages = {1648-1656}, DOI = {10.1002/chem.200500845}, keywords = {carbocations • kinetics • nucleophilic substitution • reaction mechanisms • solvent effects}, journal = {Chemistry : a European journal}, doi = {10.1002/chem.200500845}, volume = {12}, number = {6}, issn = {0947-6539}, title = {Kinetics of the Solvolyses of Benzhydryl Derivatives: Basis for the Construction of a Comprehensive Nucleofugality Scale}, keyword = {carbocations • kinetics • nucleophilic substitution • reaction mechanisms • solvent effects} }

Časopis indeksira:


  • Current Contents Connect (CCC)
  • Web of Science Core Collection (WoSCC)
    • Science Citation Index Expanded (SCI-EXP)
    • SCI-EXP, SSCI i/ili A&HCI
  • Scopus
  • MEDLINE


Uključenost u ostale bibliografske baze podataka::


  • Chemical Abstracts


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