Pregled bibliografske jedinice broj: 43798
Spirobinaphthopyrans: Synthesis, X-ray Crystal Structure, Separation of Enantiomers and Barriers to Thermal Racemization
Spirobinaphthopyrans: Synthesis, X-ray Crystal Structure, Separation of Enantiomers and Barriers to Thermal Racemization // Chirality, 11 (1999), 363-372 (međunarodna recenzija, članak, znanstveni)
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Naslov
Spirobinaphthopyrans: Synthesis, X-ray Crystal
Structure, Separation of Enantiomers and
Barriers to Thermal Racemization
Autori
Lončar-Tomašković, Linda ; Lorenz, Klaus ; Hergold-Brundić, Antonija ; Mrvoš-Sermek, Draginja ; Nagl, Ante ; Mintas, Mladen ; Mannschreck, Albrecht
Izvornik
Chirality (0899-0042) 11
(1999);
363-372
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
Chiral spirobinaphthopyrans ; enantioselective liquid chromatography ; triacetylcellulose ; barriers to racemization ; X-ray crystallography
Sažetak
Chiral spirobinaphtopyrans 1-9 were synthesised using the acid catalyzed aldol condensation of 2-hydroxy-1-naphthaldehyde or 1-hydroxy-2- naphthaldehyde with the appropriate ketone and subsequent reaction of the isolated pyrylium salt with base. Separation or enrichment of enantiomers was accomplished by low-pressure liquid chromatography (LPLC) on triacetylcellulose, tribenzoylcellulose or (+)- poly(triphenylmethyl methacrylate) on SiO2. The barriers for the interconversion of enantiomers were determined by dynamic 1H NMR measurements and by on line- or off line-measurements of the enriched enantiomers after LPLC. Gibbs energies of activation G for reversible cleavage of the Cspiro-O bond in 1 - 9 were found in the range 85-105 kJ/mol and are rationalized by steric and electronic effects. The G values decrease with decreasing length of the bridge or decreasing size of substituents in the 3- and 3'-positions. Therefore, G for 7 is higher than 9 higher than 6, 3 higher than 2 and 4 higher than 1. Geometrical data from X-ray crystal sructure analysis show that the mean value of the Cspiro-O bond length in the spirobibenzopyran 14 is shorter, i.e. the bond is stronger, than that in the spirobinaphtho derivatives 4, 3 and 6. This bond length shortening is explained by the weaker conjugation of the oxygen -lone electron pair with the -system of the benzene ring in 14 compared to the naphthalene moiety in 3, 4, and 6.
Izvorni jezik
Engleski
Znanstvena područja
Kemija
POVEZANOST RADA
Projekti:
125003
Ustanove:
Prirodoslovno-matematički fakultet, Zagreb,
Fakultet kemijskog inženjerstva i tehnologije, Zagreb
Profili:
Mladen Mintas
(autor)
Linda Tomašković
(autor)
Draginja Mrvoš-Sermek
(autor)
Antonija Hergold-Brundić
(autor)
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
- MEDLINE