160 articles for the search > VCD

Conformational Flexibility in Terpenes: Vibrational Circular Dichroism (VCD), Infrared and Raman Study of S-(−)-Perillaldehyde

2008 / The Journal of Physical Chemistry A

S-(−)-Perillaldehyde (4-isopropenylcyclohex-1-ene-1-carbaldehyde) is a secondary metabolite and an atmospheric pollutant obtained from the oxidation of other terpenes, as limonene and… Continue reading Conformational Flexibility in Terpenes: Vibrational Circular Dichroism (VCD), Infrared and Raman Study of S-(−)-Perillaldehyde

Leah Pandiscia, PhD

Supramolecular organization of perfluorinated 1H-indazoles in the solid state using X-ray crystallography, SSNMR and sensitive (VCD) and non sensitive (MIR, FIR and Raman) to chirality vibrational spectroscopies

2017 / Physical Chemistry Chemical Physics

1H-Indazole derivatives exhibit a remarkable property since some of them form chiral supramolecular structures starting from achiral monomers. The present… Continue reading Supramolecular organization of perfluorinated 1H-indazoles in the solid state using X-ray crystallography, SSNMR and sensitive (VCD) and non sensitive (MIR, FIR and Raman) to chirality vibrational spectroscopies

Leah Pandiscia, PhD

Hydrogen bonding network in a chiral alcohol: (1R,2S,5R)-(−)-menthol. Conformational preference studied by IR–Raman–VCD spectroscopies and quantum chemical calculations

2013 / Structural chemistry

A study of the molecular structure of (1R,2S,5R)-(−)-menthol and the hydrogen bond networks formed by this species in solution is… Continue reading Hydrogen bonding network in a chiral alcohol: (1R,2S,5R)-(−)-menthol. Conformational preference studied by IR–Raman–VCD spectroscopies and quantum chemical calculations

Leah Pandiscia, PhD

Conformational Flexibility in Terpenes: Vibrational Circular Dichroism (VCD), Infrared and Raman Study of S-(−)-Perillaldehyde

2008 / The Journal of Physical Chemistry A

S-(−)-Perillaldehyde (4-isopropenylcyclohex-1-ene-1-carbaldehyde) is a secondary metabolite and an atmospheric pollutant obtained from the oxidation of other terpenes, as limonene and… Continue reading Conformational Flexibility in Terpenes: Vibrational Circular Dichroism (VCD), Infrared and Raman Study of S-(−)-Perillaldehyde

Leah Pandiscia, PhD

Supramolecular organization of perfluorinated 1H-indazoles in the solid state using X-ray crystallography, SSNMR and sensitive (VCD) and non sensitive (MIR, FIR and Raman) to chirality vibrational spectroscopies

2017 / Physical Chemistry Chemical Physics

1H-Indazole derivatives exhibit a remarkable property since some of them form chiral supramolecular structures starting from achiral monomers. The present… Continue reading Supramolecular organization of perfluorinated 1H-indazoles in the solid state using X-ray crystallography, SSNMR and sensitive (VCD) and non sensitive (MIR, FIR and Raman) to chirality vibrational spectroscopies

Leah Pandiscia, PhD

Hydrogen bonding network in a chiral alcohol: (1R,2S,5R)-(−)-menthol. Conformational preference studied by IR–Raman–VCD spectroscopies and quantum chemical calculations

2013 / Structural chemistry

A study of the molecular structure of (1R,2S,5R)-(−)-menthol and the hydrogen bond networks formed by this species in solution is… Continue reading Hydrogen bonding network in a chiral alcohol: (1R,2S,5R)-(−)-menthol. Conformational preference studied by IR–Raman–VCD spectroscopies and quantum chemical calculations

Leah Pandiscia, PhD

Electronic and vibrational circular dichroism spectroscopic study of non-covalent interactions of meso-5,10,15,20-tetrakis (1-methylpyridinium-4-yl)porphyrin with (dG-dC)10 and (dA-dT)10

2007 / Vibrational Spectroscopy

The non-covalent interactions of (dG-dC)10 and (dA-dT)10 with 5,10,15,20-tetrakis(1-methylpyridinium-4-yl)porphyrin (TMPyP) were studied using the combination of electronic circular dichroism (ECD), vibrational circular… Continue reading Electronic and vibrational circular dichroism spectroscopic study of non-covalent interactions of meso-5,10,15,20-tetrakis (1-methylpyridinium-4-yl)porphyrin with (dG-dC)10 and (dA-dT)10

Leah Pandiscia, PhD

Reassignment of the absolute configuration of plakinidone from the sponge consortium Plakortis halichondrioides–Xestospongia deweerdtae using a combination of synthesis and a chiroptical approach

2016 / Tetrahedron: Asymmetry

Recent work by Wu et al. in connection with the first synthesis of the marine natural product plakinidone revealed that… Continue reading Reassignment of the absolute configuration of plakinidone from the sponge consortium Plakortis halichondrioides–Xestospongia deweerdtae using a combination of synthesis and a chiroptical approach

Leah Pandiscia, PhD

Chiral and achiral vanadyl lactates with vibrational circular dichroism: Toward the chiral metal cluster in nitrogenase

2016 / Inorganica Chimica Acta

A series of chiral and achiral neutral vanadyl complexes with N-heterocycle chelated ligands [V2O2(S-lact)2(bpy)2] (1), [V2O2(S-lact)2(phen)2] (2), [V2O2(R-lact)(S-lact)(bpy)2] (3), [V2O2(R-lact)(S-lact)(phen)2]… Continue reading Chiral and achiral vanadyl lactates with vibrational circular dichroism: Toward the chiral metal cluster in nitrogenase

Leah Pandiscia, PhD

The Role of Chirality in a Set of Key Intermediates of Pharmaceutical Interest, 3-aryl-substituted-γ-butyrolactones, evidenced by Chiral HPLC Separation and by Chiroptical Spectroscopies

2017 / Journal of Pharmaceutical and Biomedical Analysis

The enantiomers of four chiral 3-aryl-substituted-γ-butyrolactones, key intermediates for the preparation of compounds of pharmaceutical interest, were successfully isolated by… Continue reading The Role of Chirality in a Set of Key Intermediates of Pharmaceutical Interest, 3-aryl-substituted-γ-butyrolactones, evidenced by Chiral HPLC Separation and by Chiroptical Spectroscopies

Leah Pandiscia, PhD

Diagnostic Absolute Configuration Determination of Tetraphenylethene Core-Based Chiral Aggregation-Induced Emission Compounds: Particular Fingerprint Bands in Comprehensive Chiroptical Spectroscopy

2017 / The Journal of Physical Chemistry C

Tetraphenylethylene (TPE) and its derivatives are the typical aggregation-induced emission (AIE) compounds with helical chirality, and they have enormous applications… Continue reading Diagnostic Absolute Configuration Determination of Tetraphenylethene Core-Based Chiral Aggregation-Induced Emission Compounds: Particular Fingerprint Bands in Comprehensive Chiroptical Spectroscopy

Leah Pandiscia, PhD

Conformational landscape in chiral terpenes from vibrational spectroscopy and quantum chemical calculations: S-(+)-carvone

2009 / Vibrational Spectroscopy

S-(+)-carvone (5-isopropenyl-2-methylcyclohex-2-en-1-one) is the primary component in the oil of caraway. Different experimental and theoretical works reveal that there are… Continue reading Conformational landscape in chiral terpenes from vibrational spectroscopy and quantum chemical calculations: S-(+)-carvone

Carlos Morillo

Conformational landscape in chiral terpenes from vibrational spectroscopy and quantum chemical calculations: S-(+)-carvone

2009 / Vibrational Spectroscopy

S-(+)-carvone (5-isopropenyl-2-methylcyclohex-2-en-1-one) is the primary component in the oil of caraway. Different experimental and theoretical works reveal that there are… Continue reading Conformational landscape in chiral terpenes from vibrational spectroscopy and quantum chemical calculations: S-(+)-carvone

Leah Pandiscia, PhD