Pregled bibliografske jedinice broj: 43911
Chromatographic resolution, Circular Dichroism Spectra, Absolute Configurations, and Crystal Structures of Bridged Biphenyls, Containing Sulfide, Sulfoxide, and Sulfone Groups in the Bridge
Chromatographic resolution, Circular Dichroism Spectra, Absolute Configurations, and Crystal Structures of Bridged Biphenyls, Containing Sulfide, Sulfoxide, and Sulfone Groups in the Bridge // Helvetica chimica acta, 83 (2000), 2; 479-494 doi:10.1002/(SICI)1522-2675(20000216)83:23.0.CO ; 2-W (međunarodna recenzija, članak, znanstveni)
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Naslov
Chromatographic resolution, Circular Dichroism Spectra, Absolute Configurations, and Crystal Structures of Bridged Biphenyls, Containing Sulfide, Sulfoxide, and Sulfone Groups in the Bridge
Autori
Lončar-Tomašković, Linda ; Šarac-Arneri, Ruža ; Hergold-Brundić, Antonija ; Nagl, Ante ; Mintas, Mladen ; Sandström, Jan
Izvornik
Helvetica chimica acta (0018-019X) 83
(2000), 2;
479-494
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
Circular Dichroism Spectra ; Absolute Configurations ; Bridged Biphenyls ; X-ray cryctallography ; empirical force-field calculation ; CNDO/S calculation ; Enantioselective chromatography on triacetylcellulose
Sažetak
Four chiral 1, 1'-biphenyls with one or two sulfur-containing bridges in 2, 2'-or 2, 2'- and 6, 6' position, viz. 1, 11-dimethyl-5, 7-dihydrodibenzo/c, e/thiepin (1), its S-oxide (2) and S, S-dioxide (3), and the doubly bridged 10, 12-dihydro-4H, 6H-/2/benzothiepino/6, 5, 4-def//2/benzothiepin (4) have been studied by chromatography, CD spectroscopy, X-ray crystallography, and empirical force-field and CNDO/S calculations. The structures obtained by force-field calculations showed good agreement with the crystal structures determined for 2 and 3. Compounds 2, 3 and 4, but not 1, could be resolved into enantiomers by chromatography on swollen microcrystalline triacetylcellulose. The barrier for biphenyl inversion in 2 was found to be higher than 167 kJmol^-1 by an attempted thermal racemization. The CD spectra of the enantiomers of 2-4 were recorded and resolved into individual bands, and the corresponding rotational strengths were calculated. The transitions showed considerable similarity to those of a 1, 1' biphenyl with hydrocarbon bridge (cf. 5), albeit with bathochromic shifts, which permitted the assignment of the absolute configurations of the enantiomers of 2-4. The assignments were supported by comparison of the experimental CD spectra with spectra calculated by the CNDO/S method. All first-eluted enantimers were found to have the (S)-configuration.
Izvorni jezik
Engleski
Znanstvena područja
Kemija
POVEZANOST RADA
Projekti:
125003
Ustanove:
Prehrambeno-biotehnološki fakultet, Zagreb,
Prirodoslovno-matematički fakultet, Zagreb,
Fakultet kemijskog inženjerstva i tehnologije, Zagreb
Citiraj ovu publikaciju:
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