FT-IR and raman spectral evidence for metal complex formation with?-cyclodextrin as a first sphere ligand

1989 ◽  
Vol 7 (4) ◽  
pp. 455-460 ◽  
Author(s):  
Noel R. Russell ◽  
Mary McNamara
Keyword(s):  
Complex Formation ◽  
Metal Complex ◽  
Spectral Evidence ◽  
Ft Ir ◽  
Raman Spectral ◽  
Ir And Raman

FT-IR AND RAMAN SPECTROSCOPIC STUDY OF Cr2O3-TeO2-B2O3-SrF2 GLASSES

2006 ◽  
Vol 20 (18) ◽  
pp. 1107-1114 ◽  
Author(s):  
I. ARDELEAN ◽  
N. MUREŞAN ◽  
P. PǍŞCUŢǍ
Keyword(s):  
Spectroscopic Study ◽  
Local Structure ◽  
Glass System ◽  
Spectral Measurements ◽  
Structural Units ◽  
Raman Spectroscopic ◽  
Raman Spectroscopic Study ◽  
Ft Ir ◽  
Raman Spectral ◽  
Ir And Raman

Homogeneous glasses were formed in the Cr 2 O 3- TeO 2- B 2 O 3- SrF 2 system, up to 20 mol% Cr 2 O 3. For these glasses, IR and Raman spectral measurements were carried out in order to elucidate the local structure. The results showed that BO 3 and BO 4 are the main structural units of the glass system and the chromium ions are located in the network. It was evidenced the presence of TeO 3 and TeO 4 units as possible structural units in our glasses.

Solid State Analysis and Theoretical Explorations on Polymorphic and Hydrate Forms of p-Hydroxybenzaldehyde Isonicotinichydrazone: Effect of Additives on Polymorphic Crystallization

2018 ◽  
Author(s):  
Lincy Tom ◽  
Victoria A. Smolenski ◽  
Jerry P. Jasinski ◽  
M.R. Prathapachandra Kurup
Keyword(s):  
Hirshfeld Surface ◽  
Framework Analysis ◽  
Reaction Conditions ◽  
Space Groups ◽  
Effect Of Additives ◽  
Ft Ir ◽  
Packing Arrangement ◽  
The Stability ◽  
Ir And Raman ◽  
Isonicotinic Hydrazide

The reaction of p-hydroxybenzaldehyde with an equimolar amount of isonicotinic hydrazide afforded two polymorphic and hydrate forms of p-hydroxybenzaldehyde isonicotinichydrazone (HBIH) by varying the experimental reaction conditions. The compounds are fully characterized by means of single crystal and powder diffraction methods, vibrational spectroscopy (FT-IR and Raman), thermal and elemental analysis. The compound crystallizes in three different forms in two different space groups, P21/c (form PA and PB) and Pbca (PC). The Hirshfeld surface analysis shows the differences in the relative contributions of intermolecular interactions to the total Hirshfeld surface area for the HBIH molecules. The calculated pairwise interaction energies (104-116 kJ/mol) can be related to the stability of the crystals. Energy framework analysis identifies the interaction hierarchy and their topology. The geometry and conformation of the three forms are essentially similar which differ only by packing arrangement.

Solid State Analysis and Theoretical Explorations on Polymorphic and Hydrate Forms of p-Hydroxybenzaldehyde Isonicotinichydrazone: Effect of Additives on Polymorphic Crystallization

2018 ◽  
Author(s):  
Lincy Tom ◽  
Victoria A. Smolenski ◽  
Jerry P. Jasinski ◽  
M.R. Prathapachandra Kurup
Keyword(s):  
Hirshfeld Surface ◽  
Framework Analysis ◽  
Reaction Conditions ◽  
Space Groups ◽  
Effect Of Additives ◽  
Ft Ir ◽  
Packing Arrangement ◽  
The Stability ◽  
Ir And Raman ◽  
Isonicotinic Hydrazide

The reaction of p-hydroxybenzaldehyde with an equimolar amount of isonicotinic hydrazide afforded two polymorphic and hydrate forms of p-hydroxybenzaldehyde isonicotinichydrazone (HBIH) by varying the experimental reaction conditions. The compounds are fully characterized by means of single crystal and powder diffraction methods, vibrational spectroscopy (FT-IR and Raman), thermal and elemental analysis. The compound crystallizes in three different forms in two different space groups, P21/c (form PA and PB) and Pbca (PC). The Hirshfeld surface analysis shows the differences in the relative contributions of intermolecular interactions to the total Hirshfeld surface area for the HBIH molecules. The calculated pairwise interaction energies (104-116 kJ/mol) can be related to the stability of the crystals. Energy framework analysis identifies the interaction hierarchy and their topology. The geometry and conformation of the three forms are essentially similar which differ only by packing arrangement.

Molecular structure analysis of ascending aorta aneurysm upon atherosclerosis

2020 ◽  
Vol 41 (Supplement_2) ◽  
Author(s):  
I Mamarelis ◽  
V Mamareli ◽  
M Kyriakidou ◽  
O Tanis ◽  
C Mamareli ◽  
...  
Keyword(s):  
Molecular Structure ◽  
Raman Spectra ◽  
Molecular Level ◽  
Ascending Aorta ◽  
Ir And Raman Spectra ◽  
Aggregate Formation ◽  
Aorta Aneurysm ◽  
Ft Ir ◽  
Molecular Structure Analysis ◽  
Ir And Raman

Abstract Background The atherosclerotic ascending aorta could represent a potential source of emboli or could be an indicator of atherosclerosis in general with high mortality. The mechanism of aneurysm formation and atherosclerosis of the ascending aorta at the molecular level has not yet been clarified. To approach the mechanism of ascending aortic lesions and mineralization at a molecular level, we used the non-destructive FT-IR, Raman spectroscopy, SEM and Hypermicroscope. Methods Six ascending aorta biopsies were obtained from patients who underwent aortic valve replacement (AVR) cardiac surgery. CytoViva (einst inc) hyperspectral microscope was used to obtain the images of ascending aorta. The samples were dissolved in hexane on a microscope glass plate. The FT-IR and Raman spectra were recorded with Nicolet 6700 thermoshintific and micro-Raman Reinshaw (785nm, 145 mwatt), respectively. The architecture of ascending aorta biopsies was obtained by using scanning electron microscope (SEM of Fei Co) without any coating. Results FT-IR and Raman spectra showed changes arising from the increasing of lipophilic environment and aggregate formation (Fig. 1). The band at 1744 cm–1 is attributed to aldehyde CHO mode due to oxidation of lipids. The shifts of the bands of the amide I and amide II bands to lower are associated with protein damage, in agreement with SEM data. The bands at about 1170–1000 cm–1 resulted from the C-O-C of advanced glycation products as result of connecting tissues fragmentations and polymerization. The spectroscopic data were analogous with the lesions observed with SEM and hypermicroscopic images. Conclusions The present innovate molecular structure analysis showed that upon ascending aorta aneurysm development an excess of lipophilic aggregate formation and protein lesions, changing the elasticity of the aorta's wall. The released Ca2+ interacted mostly with carbonate-terminal of cellular protein chains accelerated the ascending aorta calcifications. Figure 1. FT-IR and Raman spectra Funding Acknowledgement Type of funding source: None

L-Alanyl-glycylglycine: FT-IR and Raman spectroscopic evidence for tripeptide packing in a collagenlike arrangement

Biopolymers ◽  
1984 ◽  
Vol 23 (4) ◽  
pp. 623-627 ◽  
Author(s):  
V. Renugopalakrishnan ◽  
P. H. B. Kloumann ◽  
Rajendra S. Bhatnagar
Keyword(s):  
Spectroscopic Evidence ◽  
Raman Spectroscopic ◽  
Ft Ir ◽  
Ir And Raman

Crystal Growth, Spectral, Thermal and Optical Properties of Phthalic Anhydride (PA) Single Crystal

2012 ◽  
Vol 584 ◽  
pp. 136-140 ◽  
Author(s):  
S. Janarthanan ◽  
Y.C. Rajan ◽  
R. Sugaraj Samuel ◽  
S. Pandi
Keyword(s):  
Spectral Analysis ◽  
Single Crystal ◽  
Phthalic Anhydride ◽  
Second Harmonic ◽  
Organic Crystals ◽  
X Ray Diffraction ◽  
Fundamental Wavelength ◽  
Ft Ir ◽  
Raman Spectral ◽  
Raman Spectral Analysis

ABSTRACT Organic single crystal of Phthalic Anhydride (PA) was successfully grown by slow evaporation method. The structure of the grown crystal was confirmed by X-ray diffraction analysis. FT-IR, and FT-Raman spectral analysis of the crystalline samples reveal that the crystalline sample consists of all functional groups. The placement of protons was identified from H1-NMR spectral analysis. UV-Visible and photoluminescence spectral analyses were carried out for the grown crystals. The thermal behavior was studied with TGA-DTA analyses. The existence of second harmonic generation (SHG) signal was observed using Nd:YAG laser with a fundamental wavelength of 1064 nm. Keywords: Organic crystals, NLO crystals

Digital deconvolution of IR and Raman spectral contours

1988 ◽  
Vol 48 (2) ◽  
pp. 186-190
Author(s):  
V. I. Balyavichyus ◽  
V. I. Shablinskas ◽  
L. L. Kimtis
Keyword(s):  
Raman Spectral ◽  
Ir And Raman

scholarly journals Novel solid forms of the analgesic drug ethenzamide

2014 ◽  
Vol 70 (a1) ◽  
pp. C995-C995
Author(s):  
Duane Choquesillo-Lazarte ◽  
Cristóbal Verdugo-Escamilla ◽  
Juan Manuel García-Ruiz
Keyword(s):  
Polycrystalline Material ◽  
X Ray Diffraction ◽  
Analgesic Drug ◽  
X Ray ◽  
Solution Methods ◽  
Additional Stability ◽  
Ft Ir ◽  
Model Drug ◽  
Solid Form ◽  
Ir And Raman

The interest in multicomponent solid forms has increased in the last years within the pharmaceutical industry and also the solid-state community due to the possibility of obtaining materials with new properties [1]. Crystallization strategies, supported by solvent- and solid-based techniques, have also received attention in the search and development of methodologies for the screening of multicomponent crystals. In this work, ethenzamide, an anti-inflammatory and analgesic drug, was selected as a model drug to develop cocrystals on the basis of the synthon types using a series of phenolic coformers. Ethenzamide cocrystals and cocrystal solvates have been reported recently [2,3]. Liquid Assisted Grinding (LAG) and solution methods were used as synthetic tools. Attempts to produce cocrystals by LAG and Reaction Crystallization led to the formation of polycrystalline material. The solids obtained were then characterized by powder X-ray diffraction (PXRD), FT-IR and Raman spectroscopy. Recrystallization by slow solvent evaporation was carried out when the above-referred techniques strongly suggest the formation of a new solid form. The structure of five new multicomponent solids has been determined by single crystal X-ray diffraction. Additional stability studies have been performed at controlled relative humidity conditions and followed by PXRD.

Sign in / Sign up

Export Citation Format

Share Document