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Pregled bibliografske jedinice broj: 46406

Novel chiral stationary phases comprising 2, 4-(or 2, 6)-diamino-5, 6-(or 2, 5)-dichlorobenzene-1, 3-dicarbonitrile and 1-acyl (1R, 2R)-diaminocyclohexane


Kontrec, Darko; Vinković, Vladimir; Lesac, Andreja; Šunjić, Vitomir; Aced, Ahmed
Novel chiral stationary phases comprising 2, 4-(or 2, 6)-diamino-5, 6-(or 2, 5)-dichlorobenzene-1, 3-dicarbonitrile and 1-acyl (1R, 2R)-diaminocyclohexane // Enantiomer, 5 (2000), 3-4; 333-344 (međunarodna recenzija, članak, znanstveni)


Naslov
Novel chiral stationary phases comprising 2, 4-(or 2, 6)-diamino-5, 6-(or 2, 5)-dichlorobenzene-1, 3-dicarbonitrile and 1-acyl (1R, 2R)-diaminocyclohexane
(Novel Chiral Stationary Phases Comprising 2, 4-(or 2, 6) Diamino-5, 6- (or 2, 5) dichloro-1, 3-dicyanobenzene and 1-Acyl (1R, 2R)-diaminocyclohexane)

Autori
Kontrec, Darko ; Vinković, Vladimir ; Lesac, Andreja ; Šunjić, Vitomir ; Aced, Ahmed

Izvornik
Enantiomer (1024-2430) 5 (2000), 3-4; 333-344

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

Ključne riječi
Chiral stationary phase ; enantioseparation ; 2, 4-(or 2, 6)-diamino-5, 6-(or 2, 5)-dichlorobenzene-1, 3-dicarbonitriles ; 1, 2-(1R, 2R)-diaminocyclohexane

Sažetak
Novel chiral selectors 3-5 were prepared by regio-selective nucleophilic substitution of 2, 4, 5, 6-tetrachlorobenzene-1, 3-dicarbonitrile (TCBDC, 1) at C(4) by (1R, 2R)-trans-diaminocyclohexane, followed by acylation of the intermediary 2 with carboxylic acids containing π-acid or π-basic unit. On substitution of the second chlorine atom by the spacer 3-aminopropyltriethoxysilane (APTES), a 1:1 mixture of regioisomers of N-({; ; [3, 6-dichloro-2, 4-dicyano-5- (4, 4, 4-triethoxy-4- silabutyl)- amino]phenyl}; ; amino)cyclo-hexylcarboxamides and N-(5, 6 -dichloro-2, 4-dicyano-3- (4, 4, 4-triethoxy -4-silabutyl) -amino]phenyl}; ; amino)cyclohexylcarboxamides (6/7, 8/9, 10/11) was obtained. Their covalent binding to Nucleosil 100-5 provided three new chiral stationary phases (CSP-1-CSP-3). NMR spectra of model compounds 12-14 and MM2 calculations on model compounds 15, 16 revealed π-π interactions between persubstituted benzene ring and second aromatic ring. The results of the evaluation of new CSPs in the separation of 23 test racemates by HPLC are reported. CSP-2 and CSP-3, that have lower conformational freedom than CSP-1, allow for better separation. In particular, good results are obtained in the separation of some 1, 4-benzodiazepines and open-chain aromatic amides by CSP-2 and CSP-3.

Izvorni jezik
Engleski

Znanstvena područja
Kemija



POVEZANOST RADA


Projekt / tema
00980701

Ustanove
Institut "Ruđer Bošković", Zagreb

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