Research output: Contribution to journal › Article › peer-review
Complexes PdCl2 with optically active hybrid ligands built of α-pinene and β-alanine molecules. / Kokina, T. E.; Glinskaya, L. A.; Marenin, K. S. et al.
In: Russian Journal of Coordination Chemistry/Koordinatsionnaya Khimiya, Vol. 43, No. 4, 01.04.2017, p. 213-222.Research output: Contribution to journal › Article › peer-review
}
TY - JOUR
T1 - Complexes PdCl2 with optically active hybrid ligands built of α-pinene and β-alanine molecules
AU - Kokina, T. E.
AU - Glinskaya, L. A.
AU - Marenin, K. S.
AU - Korol’kov, I. V.
AU - Naumov, D. Yu
AU - Tkachev, A. V.
AU - Larionov, S. V.
PY - 2017/4/1
Y1 - 2017/4/1
N2 - Complexes Pd(LH)Cl2 (LH is the N-derivative of β-alanine based on (–)-α-pinene) and PdLEtCl2 (LEt is ethyl ester of LH) are synthesized. The X-ray diffraction analysis (СIF file ССDC no. 1471432) shows that the single crystals of the [PdLEtCl2] complex belong to the racemate. The crystal structure contains (+)- and (–)-enantiomeric molecules of the mononuclear complex. Ligand LEt is bidentate chelating. The coordination PdCl2N2 core is a distorted square. The contacts Pd…Cl and hydrogen bonds N–H…Cl between molecules of the (+)- and (–)-enantiomers result in the formation of dimeric ensembles, which are joined into chains due to the C–H…Cl hydrogen bonds. According to the X-ray powder diffraction data, the products of the synthesis of complex [PdLEtCl2] contain both the racemate and (+)-enantiomer. The (+)-enantiomer is isolated by the recrystallization of the synthesis product. Complex Pd(LH)Cl2 is an optically active right-handed compound. According to the NMR data, complex PdLEtCl2 does not dissociate in a CDCl3 solution. The results of IR and NMR spectroscopy indicate that the molecular structure of complex Pd(LH)Cl2 is similar to that of [PdLEtCl2].
AB - Complexes Pd(LH)Cl2 (LH is the N-derivative of β-alanine based on (–)-α-pinene) and PdLEtCl2 (LEt is ethyl ester of LH) are synthesized. The X-ray diffraction analysis (СIF file ССDC no. 1471432) shows that the single crystals of the [PdLEtCl2] complex belong to the racemate. The crystal structure contains (+)- and (–)-enantiomeric molecules of the mononuclear complex. Ligand LEt is bidentate chelating. The coordination PdCl2N2 core is a distorted square. The contacts Pd…Cl and hydrogen bonds N–H…Cl between molecules of the (+)- and (–)-enantiomers result in the formation of dimeric ensembles, which are joined into chains due to the C–H…Cl hydrogen bonds. According to the X-ray powder diffraction data, the products of the synthesis of complex [PdLEtCl2] contain both the racemate and (+)-enantiomer. The (+)-enantiomer is isolated by the recrystallization of the synthesis product. Complex Pd(LH)Cl2 is an optically active right-handed compound. According to the NMR data, complex PdLEtCl2 does not dissociate in a CDCl3 solution. The results of IR and NMR spectroscopy indicate that the molecular structure of complex Pd(LH)Cl2 is similar to that of [PdLEtCl2].
KW - hybrid ligands
KW - optical activity
KW - Pd complexes
KW - pinene
KW - structure
KW - HYDROCARBONS
KW - COPPER(II)
KW - CRYSTAL
KW - COORDINATION-COMPOUNDS
KW - (+)-3-CARENE
KW - OXIMES
KW - CHIRAL PYRIDINE
KW - NITROSO CHLORIDES
UR - http://www.scopus.com/inward/record.url?scp=85018515332&partnerID=8YFLogxK
U2 - 10.1134/S1070328417030034
DO - 10.1134/S1070328417030034
M3 - Article
AN - SCOPUS:85018515332
VL - 43
SP - 213
EP - 222
JO - Russian Journal of Coordination Chemistry/Koordinatsionnaya Khimiya
JF - Russian Journal of Coordination Chemistry/Koordinatsionnaya Khimiya
SN - 1070-3284
IS - 4
ER -
ID: 10040717