%0 Generic
%A Olszewska, Teresa
%A Gdaniec, Maria
%A Połoński, Tadeusz
%D 2004
%T Planar Chiral Dianthranilide and Dithiodianthranilide Molecules:
Optical Resolution, Chiroptical Spectra, and Molecular
Self-Assembly
%U https://acs.figshare.com/articles/dataset/Planar_Chiral_Dianthranilide_and_Dithiodianthranilide_Molecules_Optical_Resolution_Chiroptical_Spectra_and_Molecular_Self_Assembly/3349213
%R 10.1021/jo035024d.s007
%2 https://ndownloader.figshare.com/files/5188525
%K Planar Chiral Dianthranilide
%K Chiroptical Spectra
%K causes racemization
%K title compounds
%K homochiral crystals
%K bond
%K 2 show
%K Optical resolution
%K chiral derivatizing agent
%K homochiral forms
%K thiobenzamide chromophores
%K enantiomer
%K CD spectra
%K racemate
%K CD spectrum
%K motif
%K DMSO solvates
%K R configuration
%K 1 D networks
%K inclusion crystallization
%X Planar chiral dianthranilide (1) was resolved to enantiomers with use of (−)-(1S,4R)-camphanoyl
chloride as a chiral derivatizing agent. The (+)-1 enantiomer was assigned the S absolute
configuration from the X-ray crystal structure of its N,N‘-dicamphanoyl derivative. Optical resolution
of dithionodianthranilide (2) was accomplished by inclusion crystallization with (R,R)-1,2-diaminocyclohexane, and the X-ray structure of the corresponding adduct revealed the (−)-2
stereoisomer has the R configuration. A slow boat-to-boat ring inversion (ΔG⧧ = 24.1 ± 0.1 kcal
mol-1) causes racemization of (+)-1 in solution as manifested by a gradual decrease of the CD
spectrum whereas, (−)-2 is configurationally stable at these conditions. The analysis of the CD
spectra of the title compounds showed that the n−π* Cotton effect signs are determined by the
helicity of the skewed benzamide and thiobenzamide chromophores. The solid-state structures of
the racemic and homochiral forms of 1 and 2 show different self-assembly patterns: the racemate
(±)-1 prefers the cyclic R22(8) hydrogen bond motif, whereas the crystalline DMSO solvates of (±)-1
and (+)-1 consist of 1D homochiral hydrogen-bonded assemblies generated by the C(6) motif. In
the case of dithionolactams (±)-2 and (−)-2 two types of 1D networks were observed: in the racemate
they are generated by the centrosymmetric R22(8) and R22(12) hydrogen bond motifs, whereas the
molecules in the homochiral crystals are connected solely with use of the strongly nonplanar R22(8)
motif.
%I ACS Publications