2011
DOI: 10.1039/c1cs15036g
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Abstract: The electronic circular dichroism (ECD) spectra of flexible molecules include the contributions of all conformers populated at the working temperature. ECD spectra of chiral substrates depend on their stereochemistry in terms of both absolute configuration, as reflected in the sign of the spectrum, and molecular conformation, which dictates the overall spectral shape (possibly including the sign) in a very sensitive manner. The unique high sensitivity of ECD towards conformation, as well as of other chiroptica… Show more

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Cited by 292 publications
(278 citation statements)
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References 55 publications
(75 reference statements)
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“…The CD spectrum of schisandrin A1 (1) was calculated by means of TDDFT method [33] using input geometries derived from an extensive conformational analysis based on a preliminary molecular-mechanics conformational search followed by DFT geometry optimizations (see Section 6) [34]. All low-energy DFT minima (relative internal energies <2 kcal/mol than the global minimum, B3LYP/6-311Gþ(d,p) level) with sizable population (>2%) at 300 K showed a consistent arrangement of the cyclooctadiene ring and the biphenyl unit, with C-10/C-15/C-16/C-5 dihedral angle around þ67 (for aS chirality).…”
Section: Circular Dichroism Analysismentioning
confidence: 99%
“…The CD spectrum of schisandrin A1 (1) was calculated by means of TDDFT method [33] using input geometries derived from an extensive conformational analysis based on a preliminary molecular-mechanics conformational search followed by DFT geometry optimizations (see Section 6) [34]. All low-energy DFT minima (relative internal energies <2 kcal/mol than the global minimum, B3LYP/6-311Gþ(d,p) level) with sizable population (>2%) at 300 K showed a consistent arrangement of the cyclooctadiene ring and the biphenyl unit, with C-10/C-15/C-16/C-5 dihedral angle around þ67 (for aS chirality).…”
Section: Circular Dichroism Analysismentioning
confidence: 99%
“…It consists of comparing the electronic circular dichroism (ECD) spectrum measured on a microcrystalline sample with that calculated by means of time-dependent density functional theory (TDDFT) [17] using the X-ray coordinates as input structure. This approach renders a full conformational analysis unnecessary [18] and is especially useful in assigning the absolute configuration of flexible natural products. In the case of compound 1, the rotation of the furan chromophore around the C17-C20 bond, which is expected to affect the ECD spectrum, is frozen in the crystals.…”
Section: Fig 2 (Color Online)mentioning
confidence: 99%
“…Due to the asymmetric spatial disposition of the sulfate groups, the intermolecularly stacked aminoquinoline rings form a supramolecular, chiral layer around the macrocycle resulting in strong exciton CD splitting of intermolecular origin. Application of the exciton coupling theory [11,12] predicts that the observed positive-negative CD feature (Fig. 1) correlates with the right-handed (P-helical) orientation of long axes of adjacent aminoquinoline moieties (linear dichroism measurements showed that in the parent 4-aminoquinoline the electronic transition moment of the main UV band centered around 221 nm is oriented along the long axis of the molecule [13]).…”
Section: Resultsmentioning
confidence: 99%