Studies on metal hydroxy compounds. II. Infrared spectra of zinc derivatives ϵ-Zn(OH)2, β-ZnOHCl, ZnOHF, Zn5(OH)8Cl2, and Zn5(OH)8Cl2·H2O

1967 ◽  
Vol 45 (6) ◽  
pp. 585-588 ◽  
Author(s):  
O. K. Srivastava ◽  
E. A. Secco
Keyword(s):  
Infrared Spectra ◽  
Group Factor ◽  
Absorption Bands ◽  
Site Group ◽  
Planar Molecule ◽  
Stretching Vibration ◽  
Hydroxy Compounds ◽  
A Site ◽  
First Time ◽  
Unambiguous Assignment

Infrared spectra of ϵ-Zn(OH)2, β-ZnOHCl, ZnOHF, Zn5(OH)8Cl2, and Zn5(OH)8Cl2·H2O and their deuterated analogues in the range 2.5–16 μ are reported for the first time. The effects of substituting a halogen for an OH group in Zn(OH)2 are (i) sharper OH stretching absorption bands, (ii) splitting of bands involving OH to give distinct doublets in ZnOHF and Zn5(OH)8Cl2, indicating strong intermolecular coupling, and (iii) shift of the OH stretching vibration to a higher frequency. Strong absorption bands are observed in the region of 695–780 cm−1 for all compounds and also near 1 020 ± 30 cm−1 in all cases except ZnOHCl. All the observed bands are displaced to lower frequencies by the deuterated analogues, with vH/vD ratios in the range 1.30–1.36. A cursory interpretation of the spectra of ZnOHCl and ZnOHF is given in terms of a planar molecule of Cs symmetry, but the unambiguous assignment of the bands must await a site group or group factor analysis.

Studies on metal hydroxy compounds. IV. Infrared spectra of cadmium derivatives Cd(OH)2, CdOHCl, and CdOHF

1967 ◽  
Vol 45 (24) ◽  
pp. 3199-3201 ◽  
Author(s):  
O. K. Srivastava ◽  
E. A. Secco
Keyword(s):  
Infrared Spectra ◽  
Strong Absorption ◽  
Lattice Vibrations ◽  
Absorption Bands ◽  
Simple Molecule ◽  
Stretching Vibration ◽  
Hydroxy Compounds ◽  
First Time ◽  
Lower Frequencies

Infrared spectra of hexagonal Cd(OH)2, CdOHCl, and CdOHF, along with deuterated analogues CdODCl and CdODF, in the range 2.5–16 μ are reported for the first time. The effects of substituting a halogen for an OH group in Cd(OH)2 are (i) shift of OH stretching vibration to a lower frequency and (ii) appearance of strong absorption bands in the region 8–16 μ. All the observed bands in the deuterated analogues are displaced to lower frequencies with νH/νd ratios between 1.35–1.37. The spectra of CdOHCl and CdOHF show a high correlation with their zinc analogues and although both spectra appear consistent with a simple molecule of Cs or C1 symmetry, an alternate interpretation is given in terms of OH lattice vibrations.

Far infrared spectra of charge-transfer complexes between iodine and substituted pyridines

1967 ◽  
Vol 297 (1451) ◽  
pp. 440-448 ◽  
Keyword(s):  
Charge Transfer ◽  
Infrared Spectra ◽  
Equilibrium Constants ◽  
Far Infrared ◽  
Charge Transfer Complexes ◽  
Absorption Bands ◽  
Substituted Pyridines ◽  
Stretching Vibration ◽  
Far Infrared Spectra ◽  
Electronic And Steric Effects

Far infrared spectra of charge-transfer complexes between iodine and substituted pyridines, dissolved in cyclohexane, have been measured in the region 20 to 200 cm -1 . Bands have been assigned to the modified iodine molecule stretching vibration near 180 cm -1 , and to the stretching of the intermolecular bond in the range 65 to 95 cm -1 . The shifts of the vibration frequencies, and force constants calculated using a simple valency force field, have been discussed in relation to the mass, electronic and steric effects of substituent groups. Equilibrium constants for the formation of the complex have been determined. From the intensities of the absorption bands, further evidence has been found for a vibronic interaction, leading to a delocalization of the transition moment in the vibrations of the complexes, and to an enhancement of the intensity of absorption.

Complexes of alkyl and aryl cyanides. Part VI. The vibrational spectra of MX2•2RCN, where M = Pd or Pt, X = Cl or Br, and R = Me or Ph, and the assignment of the metal–nitrogen stretching frequency

1968 ◽  
Vol 46 (14) ◽  
pp. 2347-2352 ◽  
Author(s):  
R. A. Walton
Keyword(s):  
Infrared Spectra ◽  
Vibrational Spectra ◽  
Metal Halide ◽  
Careful Examination ◽  
Absorption Bands ◽  
Intense Absorption ◽  
Nitrogen Bonds ◽  
Cis And Trans ◽  
First Time

A careful examination of the Raman and infrared spectra of the crystalline planar complexes cis-and trans-MX2•2RCN, where M = Pd or Pt, X = Cl or Br, and R = Me or Ph, reveals intense absorption bands in the 125–80 cm−1 region which can be assigned to modes involving stretching of the metal–nitrogen bonds. Alternative assignments for v(M—N) are also discussed. These results are compared with those for other metal halide – RCN systems. The complexes trans-PtBr2•2RCN are described for the first time.

Synthesis of Galactomannan Sulfate-Citrate

2022 ◽  
Vol 1049 ◽  
pp. 218-223
Author(s):  
Aleksandr S. Kazachenko ◽  
Yuriy N. Malyar ◽  
Anna S. Kazachenko
Keyword(s):  
Biological Activity ◽  
Ftir Spectroscopy ◽  
X Ray Diffraction ◽  
Absorption Bands ◽  
X Ray ◽  
Mixed Ester ◽  
First Time ◽  
Derivatives Of

Sulfated derivatives of polysaccharides have anticoagulant, hypolipedimic and other biological activity. In this work, a complex mixed ester of galactomannan, its sulfate-citrate, was obtained for the first time. The introduction of citrate and sulfate groups was proved by FTIR spectroscopy by the appearance of corresponding absorption bands. It was shown by X-ray diffraction that the introduction of the citrate group leads to the amorphization of the galactomannan structure.

scholarly journals The T788G Mutation in thecyp51CGene Confers Voriconazole Resistance in Aspergillus flavus Causing Aspergillosis

2012 ◽  
Vol 56 (5) ◽  
pp. 2598-2603 ◽  
Author(s):  
Wei Liu ◽  
Yi Sun ◽  
Wei Chen ◽  
Weixia Liu ◽  
Zhe Wan ◽  
...  
Keyword(s):  
Aspergillus Flavus ◽  
Resistant Strain ◽  
Antifungal Susceptibility ◽  
Gene Replacement ◽  
Content Type ◽  
Replacement Method ◽  
First Choice ◽  
The One ◽  
A Site ◽  
First Time

ABSTRACTWith voriconazole (VRC) being approved as the first choice in treating invasive aspergillosis (IA) and its increasing use in treatment, a VRC-resistant strain ofAspergillus flavus, the second leading cause of IA afterAspergillus fumigatus, has emerged. The VRC-resistant strain ofA. flavuswas isolated for the first time from the surgical lung specimen of an IA patient with no response to VRC therapy. In order to ascertain the mechanism of VRC resistance, the azole target enzyme genes in this strain ofA. flavuswere cloned and sequenced, and 4 mutations generating amino acid residue substitutions were found in thecyp51Cgene. To further determine the role of this mutated gene for VRC resistance inA. flavus, anAgrobacterium tumefaciens-mediated gene replacement approach was applied. Consequently, the mutatedcyp51Cgene from thisA. flavusstrain was proven to confer the VRC resistance. Finally, to discern the one out of the four mutations in thecyp51Cgene that is responsible for contributing to VRC resistance, a site-directed gene mutagenesis procedure combined with a gene replacement method was performed. As a result, the T788G missense mutation in thecyp51Cgene was identified as responsible for VRC resistance inA. flavus. These findings indicated that the detection of this mutation inA. flavuscould serve as an indicator for physicians to avoid the use of VRC during IA treatment. Further comprehensive surveillance for antifungal susceptibility, as well as intensive study on the mechanism of azole resistance inA. flavuscausing IA, would be required to fully understand this mechanism.

Pyrrole Studies. I. The Infrared Spectra of 2-Monosubstituted Pyrroles

1963 ◽  
Vol 16 (1) ◽  
pp. 93 ◽  
Author(s):  
RA Jones
Keyword(s):  
Infrared Spectra ◽  
Infrared Absorption ◽  
Absorption Bands ◽  
Infrared Absorption Bands

The positions and intensities of the characteristic infrared absorption bands of the nucleus are recorded and discussed for thirty-five 2-monosubstituted pyrroles.

Studies on metal hydroxy compounds. X. Thermal analyses, decomposition kinetics, and infrared spectra of lead halide (Cl, Br, I) derivatives

1970 ◽  
Vol 48 (16) ◽  
pp. 2617-2622 ◽  
Author(s):  
P. Ramamurthy ◽  
E. A. Secco ◽  
M. Badri
Keyword(s):  
Infrared Spectra ◽  
Rate Equation ◽  
Thermal Analyses ◽  
Decomposition Reaction ◽  
Diffusion Type ◽  
Type Rate ◽  
Hydroxy Compounds ◽  
Kinetics Of ◽  
Lead Halide ◽  
Order Rate Equation

The thermal analyses, thermogravimetry (TG), and differential thermal analysis (DTA) of PbOHCl, PbOHBr, and PbOHI reveal that the initial mode of decomposition is via dehydroxylation. Calorimetric measurements along with related enthalpy values for the decomposition reaction are given.The infrared spectra of these compounds are interpreted in terms of folded bands of (PbOH+)n tied together by halide ions consistent with their crystal structures.The kinetics of thermal decomposition of lead hydroxyhalides follow a diffusion-type rate equation which is in contrast to the simple first-order rate equation observed for most Cd, Zn, and Cu compounds. These two distinct rates are interpreted in terms of mobile OH or H species in the dehydroxylation step.

scholarly journals Seed Mediated Synthesis of Colloidal Halide Perovskite Nanoplatelets

2021 ◽  
Author(s):  
C. Meric Guvenc ◽  
sinan balci
Keyword(s):  
Optical Properties ◽  
Halide Salt ◽  
Seed Solution ◽  
Synthesis Route ◽  
Line Widths ◽  
Halide Perovskite ◽  
Seed Mediated ◽  
A Site ◽  
First Time ◽  
Lead Halide

<p><b>Two-dimensional lead halide perovskite nanoplatelets (2D LHP NPLs) have been emerging as one of the most promising semiconductor nanomaterials due to their narrow absorption and emission line widths, tunable bandgaps, high exciton binding energies, high defect tolerance as well as highly localized energy states. Colloidal synthesis of 2D LHP NPLs is generally performed using hot-injection or ligand assisted precipitation techniques (LARP). In the LARP method, perovskites are synthesized in polar solvents, which decrease the stability of the 2D LHP NPLs due to their weakly bonded nature. In fact, the presence of residual polar solvent in the LHP NPL colloid can cause deterioration of thickness uniformity, degradation of NPLs to parent precursors, and undesired phase transformations. Herein, for the first time, we report facile seed-mediated synthesis route of monolayer, 2-monolayers, and thicker lead halide perovskite nanoplatelets without using A site cation halide salt (AX</b><b>;</b><b> A = Cesium, methylammonium, formamidinium and, X = Cl, Br, I) and long chain alkylammonium halide salts (LX; L = oleylammonium, octylammonium, butylammonium and, X = Cl, Br, I). The seed solution has been synthesized by reacting lead (II) halide salt and coordinating ligands (oleylamine or octylamine and oleic acid) in nonpolar high boiling solvent (1-octadecene). The seed mediated synthesis has been carried out in hexane by reacting seed solution with A-site cation precursors (Cs-oleate, FA-oleate, or diluted MA solution in hexane) under ambient conditions. More importantly, the seed mediated growth of NPLs has been tracked for the first time by performing in-situ optical measurements. Furthermore, the optical properties and morphologies of the seeds have been extensively studied. We find that our facile synthesis route provides highly stable, monodisperse NPLs with narrow absorption, and photoluminescence line widths (68-201 meV), and high PLQY (37.6-1.66% for 2ML NPLs). Furthermore, anion exchange reactions have been performed by mixing pre-synthesized LHP NPLs with counter halide seeds. The optical properties of NPLs have been affectively tuned by postsynthetic chemical reactions without changing the thickness of the NPLs. We anticipate that our new synthetic route provides further understanding of growth dynamics of LHP NPLs.</b></p>

scholarly journals THE USE OF INFRARED SPECTROPHOTOMETRY FOR THE ESTIMATION OF SMALL QUANTITIES OF SOME HALOGENATED HYDROCARBONS

1953 ◽  
Vol 31 (4) ◽  
pp. 328-337 ◽  
Author(s):  
L. Breitman ◽  
E. W. R. Steacie
Keyword(s):  
Quantitative Analysis ◽  
Carbon Tetrachloride ◽  
Gas Phase ◽  
Infrared Spectra ◽  
Methyl Chloride ◽  
Ternary Mixtures ◽  
Halogenated Hydrocarbons ◽  
Infrared Spectrophotometry ◽  
Absorption Bands ◽  
Binary And Ternary Mixtures

The infrared spectra of chloral, carbon tetrachloride, and chloroform have been determined between 1500 and 650 cm.−1 over a range of pressures in the gas phase. Absorption bands suitable for the quantitative analysis of binary and ternary mixtures of the components have been selected and their peak intensities shown to obey Beer's Law over the range of pressures studied. Ternary mixtures have been analyzed from the spectra with an accuracy of about 20%.The spectra of dichloromethane and methyl chloride have also been measured under comparable conditions.

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