Origin of Anomalous Electronic Circular Dichroism Spectrum of RuPt2(tppz)2Cl2(PF6)4 in Acetonitrile

2014 ◽  
Vol 118 (29) ◽  
pp. 5400-5406
Author(s):  
Hua-Gen Yu
Keyword(s):  
Circular Dichroism ◽  
Circular Dichroism Spectrum ◽  
Electronic Circular Dichroism ◽  
Circular Dichroïsm

Theoretical simulation of the electronic circular dichroism spectrum of calicheamicin

2005 ◽  
Vol 13 (17) ◽  
pp. 5072-5079 ◽  
Author(s):  
Egidio Giorgio ◽  
Katsunori Tanaka ◽  
Weidong Ding ◽  
Girija Krishnamurthy ◽  
Keith Pitts ◽  
...  
Keyword(s):  
Circular Dichroism ◽  
Circular Dichroism Spectrum ◽  
Electronic Circular Dichroism ◽  
Theoretical Simulation ◽  
Circular Dichroïsm

The shape of the electronic circular dichroism spectrum of (2,6-dimethylphenyl)(phenyl)methanol: interplay between conformational equilibria and vibronic effects

2017 ◽  
Vol 19 (48) ◽  
pp. 32349-32360 ◽  
Author(s):  
Daniele Padula ◽  
Javier Cerezo ◽  
Gennaro Pescitelli ◽  
Fabrizio Santoro
Keyword(s):  
Circular Dichroism ◽  
Solvent Effects ◽  
Circular Dichroism Spectrum ◽  
Electronic Circular Dichroism ◽  
Conformational Equilibria ◽  
Circular Dichroïsm ◽  
Vibronic Effects

Analysis of the interplay between conformational equilibria, solvent effects and vibronic contributions in the ECD spectra.

Analysis of the Electronic Circular Dichroism Spectrum of (−)-[9](2,5)Pyridinophane

Chirality ◽  
2012 ◽  
Vol 24 (12) ◽  
pp. 994-1004 ◽  
Author(s):  
Daniele Padula ◽  
Lorenzo Di Bari ◽  
Fabrizio Santoro ◽  
Hans Gerlach ◽  
Antonio Rizzo
Keyword(s):  
Circular Dichroism ◽  
Circular Dichroism Spectrum ◽  
Electronic Circular Dichroism ◽  
Circular Dichroïsm

scholarly journals Mass-resolved electronic circular dichroism ion spectroscopy

Science ◽  
2020 ◽  
Vol 368 (6498) ◽  
pp. 1465-1468 ◽  
Author(s):  
Steven Daly ◽  
Frédéric Rosu ◽  
Valérie Gabelica
Keyword(s):  
Circular Dichroism ◽  
Three Dimensional ◽  
Polarized Light ◽  
Negative Ions ◽  
Data Interpretation ◽  
Electronic Circular Dichroism ◽  
Circularly Polarized Light ◽  
Chiral Compounds ◽  
Electron Photodetachment ◽  
Circular Dichroïsm

DNA and proteins are chiral: Their three-dimensional structures cannot be superimposed with their mirror images. Circular dichroism spectroscopy is widely used to characterize chiral compounds, but data interpretation is difficult in the case of mixtures. We recorded the electronic circular dichroism spectra of DNA helices separated in a mass spectrometer. We studied guanine-rich strands having various secondary structures, electrosprayed them as negative ions, irradiated them with an ultraviolet nanosecond optical parametric oscillator laser, and measured the difference in electron photodetachment efficiency between left and right circularly polarized light. The reconstructed circular dichroism ion spectra resembled those of their solution-phase counterparts, thereby allowing us to assign the DNA helical topology. The ability to measure circular dichroism directly on biomolecular ions expands the capabilities of mass spectrometry for structural analysis.

Chemical Constituents from Chloranthus elatior and Their Inhibitory Effect on Human Dihydroorotate Dehydrogenase

Planta Medica ◽  
2021 ◽  
Author(s):  
Qian Yang ◽  
An Jia ◽  
Xizi Liu ◽  
Shiyi Han ◽  
Siyang Fan
Keyword(s):  
Circular Dichroism ◽  
Chemical Constituents ◽  
Inhibitory Effect ◽  
Mass Spectrometric ◽  
Dihydroorotate Dehydrogenase ◽  
Active Compounds ◽  
Electronic Circular Dichroism ◽  
Aerial Parts ◽  
Ic50 Values ◽  
Circular Dichroïsm

AbstractA new sesquiterpene, chlorantholide G (1), a new sesquiterpene dimer, elatiolactone (2), and 2 new diterpenes, elatiorlabdane B (3) and elatiorlabdane C (4), together with 51 known compounds, were isolated from the aerial parts of Chloranthus elatior. The new structures including their absolute configurations were mainly established by mass spectrometric, NMR, and electronic circular dichroism experiments. All isolated compounds were tested for their anti-hDHODH activity. (4S,6R)-4-hydroxy-6-isopropyl-3-methylcyclohex-2-enone (5) and (4S,5R,9S,10R)-8(17),12,14-labdatrien-18-oic acid (29) were the most active compounds with IC50 values of 18.7 and 30.7 µM, respectively.

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