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Pregled bibliografske jedinice broj: 43798

Spirobinaphthopyrans: Synthesis, X-ray Crystal Structure, Separation of Enantiomers and Barriers to Thermal Racemization


Lončar-Tomašković, Linda; Lorenz, Klaus; Hergold-Brundić, Antonija; Mrvoš-Sermek, Draginja; Nagl, Ante; Mintas, Mladen; Mannschreck, Albrecht
Spirobinaphthopyrans: Synthesis, X-ray Crystal Structure, Separation of Enantiomers and Barriers to Thermal Racemization // Chirality, 11 (1999), 363-372 (međunarodna recenzija, članak, znanstveni)


CROSBI ID: 43798 Za ispravke kontaktirajte CROSBI podršku putem web obrasca

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

Citiraj ovu publikaciju:

Lončar-Tomašković, Linda; Lorenz, Klaus; Hergold-Brundić, Antonija; Mrvoš-Sermek, Draginja; Nagl, Ante; Mintas, Mladen; Mannschreck, Albrecht
Spirobinaphthopyrans: Synthesis, X-ray Crystal Structure, Separation of Enantiomers and Barriers to Thermal Racemization // Chirality, 11 (1999), 363-372 (međunarodna recenzija, članak, znanstveni)
Lončar-Tomašković, L., Lorenz, K., Hergold-Brundić, A., Mrvoš-Sermek, D., Nagl, A., Mintas, M. & Mannschreck, A. (1999) Spirobinaphthopyrans: Synthesis, X-ray Crystal Structure, Separation of Enantiomers and Barriers to Thermal Racemization. Chirality, 11, 363-372.
@article{article, author = {Lon\v{c}ar-Toma\v{s}kovi\'{c}, Linda and Lorenz, Klaus and Hergold-Brundi\'{c}, Antonija and Mrvo\v{s}-Sermek, Draginja and Nagl, Ante and Mintas, Mladen and Mannschreck, Albrecht}, year = {1999}, pages = {363-372}, keywords = {Chiral spirobinaphthopyrans, enantioselective liquid chromatography, triacetylcellulose, barriers to racemization, X-ray crystallography}, journal = {Chirality}, volume = {11}, issn = {0899-0042}, title = {Spirobinaphthopyrans: Synthesis, X-ray Crystal Structure, Separation of Enantiomers and Barriers to Thermal Racemization}, keyword = {Chiral spirobinaphthopyrans, enantioselective liquid chromatography, triacetylcellulose, barriers to racemization, X-ray crystallography} }
@article{article, author = {Lon\v{c}ar-Toma\v{s}kovi\'{c}, Linda and Lorenz, Klaus and Hergold-Brundi\'{c}, Antonija and Mrvo\v{s}-Sermek, Draginja and Nagl, Ante and Mintas, Mladen and Mannschreck, Albrecht}, year = {1999}, pages = {363-372}, keywords = {Chiral spirobinaphthopyrans, enantioselective liquid chromatography, triacetylcellulose, barriers to racemization, X-ray crystallography}, journal = {Chirality}, volume = {11}, issn = {0899-0042}, title = {Spirobinaphthopyrans: Synthesis, X-ray Crystal Structure, Separation of Enantiomers and Barriers to Thermal Racemization}, keyword = {Chiral spirobinaphthopyrans, enantioselective liquid chromatography, triacetylcellulose, barriers to racemization, X-ray crystallography} }

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





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