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Pregled bibliografske jedinice broj: 210148

13C NMR Spectra of some Simetrically 2, 2’ -Disubstituted Stlbenes: Conjugational and Conformational Effects


Vikić-Topić, Dražen; Mintas, Mladen; Raos, Nenad
13C NMR Spectra of some Simetrically 2, 2’ -Disubstituted Stlbenes: Conjugational and Conformational Effects // Journal of molecular structure, 267 (1992), 405-410 doi:10.1016/0022-2860(92)87064-3 (međunarodna recenzija, članak, znanstveni)


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Naslov
13C NMR Spectra of some Simetrically 2, 2’ -Disubstituted Stlbenes: Conjugational and Conformational Effects
(13C NMR Spectra of some Simetrically 2, 2’ -Disubstituted Stlbenes: Conjugational and Conformational Effects13C NMR Spectra of some Simetrically 2, 2’ -Disubstituted Stlbenes: Conjugational and Conformational Effects)

Autori
Vikić-Topić, Dražen ; Mintas, Mladen ; Raos, Nenad

Izvornik
Journal of molecular structure (0022-2860) 267 (1992); 405-410

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

Ključne riječi
2 ; 2’ -disubstituted cis-stilbenes ; 13C NMR Spectra ; Conjugational and Conformational Analysis

Sažetak
In the 13C NMR spectra of symmetrically 2, 2’ -disubstituted cis-stilbenes the decrease of alpha-effects and increase of gamma-effects at ortho-carbons with respect to trans-isomers were observed. However, the most significant differences in substituent effects between trans- and cis-isomers were founf for gamma-effects, at unsubstituted ortho-C-6 and C-4 atoms. The one bond C-H splitting of olefinic carbons is greater in cis-than trans-stilbenes. The differences in substituent effects and apparent coupling constants are asumed to originate mainly from the different conjugational interactions in cis- and trans-stilbenes. The conformational and configurational differences of these molecules were substantiated by molecular mechanics calculations.

Izvorni jezik
Engleski

Znanstvena područja
Kemija



POVEZANOST RADA


Ustanove:
Fakultet kemijskog inženjerstva i tehnologije, Zagreb

Profili:

Avatar Url Nenad Raos (autor)

Avatar Url Mladen Mintas (autor)

Avatar Url Dražen Vikić-Topić (autor)

Poveznice na cjeloviti tekst rada:

doi www.sciencedirect.com

Citiraj ovu publikaciju:

Vikić-Topić, Dražen; Mintas, Mladen; Raos, Nenad
13C NMR Spectra of some Simetrically 2, 2’ -Disubstituted Stlbenes: Conjugational and Conformational Effects // Journal of molecular structure, 267 (1992), 405-410 doi:10.1016/0022-2860(92)87064-3 (međunarodna recenzija, članak, znanstveni)
Vikić-Topić, D., Mintas, M. & Raos, N. (1992) 13C NMR Spectra of some Simetrically 2, 2’ -Disubstituted Stlbenes: Conjugational and Conformational Effects. Journal of molecular structure, 267, 405-410 doi:10.1016/0022-2860(92)87064-3.
@article{article, author = {Viki\'{c}-Topi\'{c}, Dra\v{z}en and Mintas, Mladen and Raos, Nenad}, year = {1992}, pages = {405-410}, DOI = {10.1016/0022-2860(92)87064-3}, keywords = {2, 2’ -disubstituted cis-stilbenes, 13C NMR Spectra, Conjugational and Conformational Analysis}, journal = {Journal of molecular structure}, doi = {10.1016/0022-2860(92)87064-3}, volume = {267}, issn = {0022-2860}, title = {13C NMR Spectra of some Simetrically 2, 2’ -Disubstituted Stlbenes: Conjugational and Conformational Effects}, keyword = {2, 2’ -disubstituted cis-stilbenes, 13C NMR Spectra, Conjugational and Conformational Analysis} }
@article{article, author = {Viki\'{c}-Topi\'{c}, Dra\v{z}en and Mintas, Mladen and Raos, Nenad}, year = {1992}, pages = {405-410}, DOI = {10.1016/0022-2860(92)87064-3}, keywords = {2, 2’ -disubstituted cis-stilbenes, 13C NMR Spectra, Conjugational and Conformational Analysis}, journal = {Journal of molecular structure}, doi = {10.1016/0022-2860(92)87064-3}, volume = {267}, issn = {0022-2860}, title = {13C NMR Spectra of some Simetrically 2, 2’ -Disubstituted Stlbenes: Conjugational and Conformational Effects13C NMR Spectra of some Simetrically 2, 2’ -Disubstituted Stlbenes: Conjugational and Conformational Effects}, keyword = {2, 2’ -disubstituted cis-stilbenes, 13C NMR Spectra, Conjugational and Conformational Analysis} }

Časopis indeksira:


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


Citati:





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