Raman studies of cyanate: Fermi resonance, hydration and hydrolysis to urea

1993 ◽  
Vol 71 (10) ◽  
pp. 1764-1773 ◽  
Author(s):  
Murray H. Brooker ◽  
Nanping Wen

Raman spectra were measured for potassium cyanate in the solid phase and as aqueous solutions in H2O and D2O for freshly prepared and for aged solutions. The results indicated that the assignment of the Fermi doublet, ν1 and 2ν2, for solid potassium cyanate was reversed from the assignment for the aqueous solution. The Fermi doublet has an associated pair of hot bands at 1191 and 1315 cm−1 which originate from the 638 cm−1 ν2 state, 010. Assignment of the hot bands was confirmed by studies of solid potassium cyanate at liquid-N2 temperature, room temperature, and at 473 K. Raman spectra of aged aqueous potassium cyanate revealed that the cyanate ion hydrolyzed slowly and spontaneously at room temperature (even without added ammonium) to produce urea and a carbamate, carbonate equilibrium mixture in parallel reactions. Hydrolysis of cyanate in aqueous ammonium chloride solution resulted in almost total conversion of cyanate to urea. The reaction was not reversible under ambient conditions. Differences in peak frequencies and half-widths were observed for the cyanate dissolved in H2O compared to solutions in D2O. The results provide evidence for strong hydrogen bonding of cyanate to water and are consistent with greater structure in the D2O solution. Theoretical ab initio calculations indicated that the water molecules hydrogen bond well at both the oxygen and nitrogen atoms of cyanate although the hydrogen bond to nitrogen was found to be slightly stronger.

1991 ◽  
Vol 69 (11) ◽  
pp. 1774-1780 ◽  
Author(s):  
A. M. Heyns ◽  
K.-J. Range ◽  
K. Müller

KHCOO II is orthorhombic at ambient conditions and it is shown that traces of moisture affect the polymorphism of these very hygroscopic crystals. Dry KHCOO II transforms into phase I at 417 K (144 °C), and this phase can be supercooled to room temperature, remaining metastable for several days before transforming back to the orthorhombic phase II. The Raman spectra of phases I and II, as well as of supercooled phase I, are reported in the present study. The absence of some prominent translational modes in the Raman spectra of KHCOO II, compared to NaHCOO II, can be explained on the basis of a group-theoretical treatment. From the temperature dependence of the linewidths of various Raman-active librational and internal modes, activation energies are obtained for intramolecular motions of the formate ions. Fermi resonance occurs between the overtone of the bending mode 2ν5 and the C—H stretching mode ν1 in KHCOO II and the coupling constant W increases with temperature. The Raman and X-ray data show that KHCOO I is structurally different from NaCHOO I, but it is not possible to assign a definite structure to this phase on the basis of a Raman spectrum alone. Key words: Potassium formate, phase transition, Raman spectra.


2021 ◽  
Vol 11 (4) ◽  
pp. 1601
Author(s):  
Henrik Palmelund ◽  
Jukka Rantanen ◽  
Korbinian Löbmann

Deep eutectic solvents (DESs) are formed by a hydrogen bond donor and an acceptor. The hydrogen bond interactions between these two components significantly depress the melting temperature of the mixture. DESs have been used as an alternative for organic solvents in various branches of the chemical industry. Many DESs are very hygroscopic and water is known to change the properties of DESs, but there has neven been a systematic study performed on the deliquesence behavior of DESs. Therefore, this study investigated the thermal and deliquescent behavior of four DESs. The DES mixtures were stored in desiccators at different relative humidities (RH) to investigate the critical RH (RH0) for deliquescence. It was found that, due to the formation of a eutonic mixture, the RH0 to induce deliquescence for a given DES mixture was lower compared to the individual components comprising the DES. The results showed that, even though all investigated DESs had eutectic melting temperatures above room temperature, but due to the low RH0, they were able to appear liquid at room temperature under ambient conditions. The eutonic and eutectic compositions were identified at different compositions for the DESs. The results emphasize that great care must be taken to control the process and storage conditions for DESs.


1993 ◽  
Vol 71 (10) ◽  
pp. 1728-1733 ◽  
Author(s):  
Richard J. Bartholomew ◽  
Donald E. Irish

Raman spectra of the formate anion in water (H2O and D2O) have been measured for four concentrations under ambient conditions and for two concentrations at temperatures ranging from 49 to 239 °C and a pressure of 10 MPa. Five of the six fundamental modes of vibration are polarized. This result is inconsistent with C2ν symmetry. The Fermi resonance doublet clearly results from the interaction of 2ν5 and ν1. The latter mode decreases in frequency as the temperature rises, thus increasing the coupling and hence the intensity of the 2ν5 component. The coupling constant, W, and the positions of the unperturbed bands [Formula: see text] and [Formula: see text] have been calculated. No evidence to support a bifurcated structure for the solvated anion was found.


1994 ◽  
Vol 72 (4) ◽  
pp. 1099-1106 ◽  
Author(s):  
Nanping Wen ◽  
Murray H. Brooker

Raman spectra of aqueous solutions of potassium cyanate have been obtained at suitable time intervals. It was found that the peaks attributed to cyanate became less intense, while the peaks attributed to urea, carbamate and carbonate, centred at 1003, 1034, and 1065 cm−1, respectively, enhanced greatly with the passage of time. Further Raman spectroscopic studies revealed that the cyanate ion hydrolysed slowly and spontaneously at room temperature. Urea, carbamate, and carbonate were formed even without additional ammonium. Raman intensity measurements were used to monitor species concentrations as a function of time. The results suggested a complicated hydrolysis process: the hydrolysis of cyanate ion to form carbonate and ammonium, a rearrangement type reaction of aqueous cyanate ion with aqueous ammonium to formed urea, and an equilibrium reaction of carbonate and ammonium to form carbamate. The initial hydrolysis of cyanate with pure water was found to be first order with rate constant k1 = (2.67 ± 0.53) × 10−4 min−1 at 22 °C. The reaction of cyanate with aqueous ammonium was found to be second order with rate constant k2 = (4.64 ± 0.93) × 10−4 mol−1•L•min−1. The equilibrium reaction of carbonate and ammonium to form carbamate was very fast. Urea and carbamate were formed in parallel reactions. It was not possible to convert urea to carbamate or carbamate to urea at room temperature.


Molecules ◽  
2021 ◽  
Vol 26 (22) ◽  
pp. 6938
Author(s):  
Chunyang Li ◽  
Chunhong Tan ◽  
Juan Zhou ◽  
Yan-Yong Lin ◽  
Xiao-Feng Wang

Under ambient conditions or 160 °C, two supramolecular isomers, namely [(H4PTTA)(H2O)2(DMF)] and [(H4PTTA)(H2O)3]··Guest (1-L and 1-H, H4PTTA = N-phenyl-N′-phenyl bicyclo[2.2.2]oct-7-ene-2,3,5,6-tetracarboxdiimide tetra-carboxylic acid, Guest = DMF and H2O), were obtained through the reaction of H4PTTA in a mixture of H2O and dimethylformamide. The single crystal structures reveal the temperature-dependent supramolecular isomerism derived from the torsion of semi-rigid of H4PTTA. The 1-L prepared at room temperature is a hydrogen bond based achiral layer, while the hydrothermal synthesized 1-H is isomer resulted in an H-bond-based chiral tubes-packed supramolecular framework.


Author(s):  
T. Baird ◽  
J.R. Fryer ◽  
S.T. Galbraith

Introduction Previously we had suggested (l) that the striations observed in the pod shaped crystals of β FeOOH were an artefact of imaging in the electron microscope. Contrary to this adsorption measurements on bulk material had indicated the presence of some porosity and Gallagher (2) had proposed a model structure - based on the hollandite structure - showing the hollandite rods forming the sides of 30Å pores running the length of the crystal. Low resolution electron microscopy by Watson (3) on sectioned crystals embedded in methylmethacrylate had tended to support the existence of such pores.We have applied modern high resolution techniques to the bulk crystals and thin sections of them without confirming these earlier postulatesExperimental β FeOOH was prepared by room temperature hydrolysis of 0.01M solutions of FeCl3.6H2O, The precipitate was washed, dried in air, and embedded in Scandiplast resin. The sections were out on an LKB III Ultramicrotome to a thickness of about 500Å.


1994 ◽  
Vol 48 (7) ◽  
pp. 875-883 ◽  
Author(s):  
Daniel R. Lombardi ◽  
Chao Wang ◽  
Bin Sun ◽  
Augustus W. Fountain ◽  
Thomas J. Vickers ◽  
...  

Raman spectra have been measured for a number of nitrates, nitrites, sulfates, ferrocyanides, and ferricyanides, both in the solid phase and in aqueous solution. Accurate locations of peak maxima are given. Limits of detection for some of the compounds are given for solutions and for solid mixtures in NaNO3. Preliminary measurements have been made on core material recovered from the storage tanks on the Hanford site in Richland, Washington. Representative spectra are presented, showing that it is possible to observe responses of individual components from measurements made directly on untreated cores, with the use of a fiberoptic sampling probe.


Molecules ◽  
2021 ◽  
Vol 26 (13) ◽  
pp. 4022
Author(s):  
Kende Attila Béres ◽  
István E. Sajó ◽  
György Lendvay ◽  
László Trif ◽  
Vladimir M. Petruševski ◽  
...  

An aerial humidity-induced solid-phase hydrolytic transformation of the [Zn(NH3)4]MoO4@2H2O (compound 1@2H2O) with the formation of [(NH4)xH(1−x)Zn(OH)(MoO4)]n (x = 0.92–0.94) coordination polymer (formally NH4Zn(OH)MoO4, compound 2) is described. Based on the isostructural relationship, the powder XRD indicates that the crystal lattice of compound 1@2H2O contains a hydrogen-bonded network of tetraamminezinc (2+) and molybdate (2−) ions, and there are cavities (O4N4(μ-H12) cube) occupied by the two water molecules, which stabilize the crystal structure. Several observations indicate that the water molecules have no fixed positions in the lattice voids; instead, the cavity provides a neighborhood similar to those in clathrates. The @ symbol in the notation is intended to emphasize that the H2O in this compound is enclathrated rather than being water of crystallization. Yet, signs of temperature-dependent dynamic interactions with the wall of the cages can be detected, and 1@2H2O easily releases its water content even on standing and yields compound 2. Surprisingly, hydrolysis products of 1 were observed even in the absence of aerial humidity, which suggests a unique solid-phase quasi-intramolecular hydrolysis. A mechanism involving successive substitution of the ammonia ligands by water molecules and ammonia release is proposed. An ESR study of the Cu-doped compound 2 (2#dotCu) showed that this complex consists of two different Cu2+(Zn2+) environments in the polymeric structure. Thermal decomposition of compounds 1 and 2 results in ZnMoO4 with similar specific surface area and morphology. The ZnMoO4 samples prepared from compounds 1 and 2 and compound 2 in itself are active photocatalysts in the degradation of Congo Red dye. IR, Raman, and UV studies on compounds 1@2H2O and 2 are discussed in detail.


2021 ◽  
Author(s):  
Wenjing Li ◽  
Shun Li ◽  
Lihua Luo ◽  
Yichen Ge ◽  
Jiaqi Xu ◽  
...  

The catalyst-free oxidative cleavage of (Z)-triaryl-substituted alkenes bearing pyridyl motif with ambient air under irradiation of blue LED at room temperature has been developed. The reaction was facile and scalable,...


2020 ◽  
Vol 5 (1) ◽  
Author(s):  
Jean-Philippe Sinnes ◽  
Ulrike Bauder-Wüst ◽  
Martin Schäfer ◽  
Euy Sung Moon ◽  
Klaus Kopka ◽  
...  

Abstract Background The AAZTA chelator and in particular its bifunctional derivative AAZTA5 was recently investigated to demonstrate unique capabilities to complex diagnostic and therapeutic trivalent radiometals under mild conditions. This study presents a comparison of 68Ga, 44Sc and 177Lu-labeled AAZTA5-PSMA-617 with DOTA-PSMA-617 analogues. We evaluated the radiolabeling characteristics, in vitro stability of the radiolabeled compounds and evaluated their binding affinity and internalization behavior on LNCaP tumor cells in direct comparison to the radiolabeled DOTA-conjugated PSMA-617 analogs. Results AAZTA5 was synthesized in a five-step synthesis and coupled to the PSMA-617 backbone on solid phase. Radiochemical evaluation of AAZTA5-PSMA-617 with 68Ga, 44Sc and 177Lu achieved quantitative radiolabeling of > 99% after less than 5 min at room temperature. Stabilities against human serum, PBS buffer and EDTA and DTPA solutions were analyzed. While there was a small degradation of the 68Ga complex over 2 h in human serum, PBS and EDTA/DTPA, the 44Sc and 177Lu complexes were stable at 2 h and remained stable over 8 h and 1 day. For all three compounds, i.e. [natGa]Ga-AAZTA5-PSMA-617, [natSc]Sc-AAZTA5-PSMA-617 and [natLu]Lu-AAZTA5-PSMA-617, in vitro studies on PSMA-positive LNCaP cells were performed in direct comparison to radiolabeled DOTA-PSMA-617 yielding the corresponding inhibition constants (Ki). Ki values were in the range of 8–31 nM values which correspond with those of [natGa]Ga-DOTA-PSMA-617, [natSc]Sc-DOTA-PSMA-617 and [natLu]Lu-DOTA-PSMA-617, i.e. 5–7 nM, respectively. Internalization studies demonstrated cellular membrane to internalization ratios for the radiolabeled 68Ga, 44Sc and 177Lu-AAZTA5-PSMA-617 tracers (13–20%IA/106 cells) in the same range as the ones of the three radiolabeled DOTA-PSMA-617 tracers (17–20%IA/106 cells) in the same assay. Conclusions The AAZTA5-PSMA-617 structure proved fast and quantitative radiolabeling with all three radiometal complexes at room temperature, excellent stability with 44Sc, very high stability with 177Lu and medium stability with 68Ga in human serum, PBS and EDTA/DTPA solutions. All three AAZTA5-PSMA-617 tracers showed binding affinities and internalization ratios in LNCaP cells comparable with that of radiolabeled DOTA-PSMA-617 analogues. Therefore, the exchange of the chelator DOTA with AAZTA5 within the PSMA-617 binding motif has no negative influence on in vitro LNCaP cell binding characteristics. In combination with the faster and milder radiolabeling features, AAZTA5-PSMA-617 thus demonstrates promising potential for in vivo application for theranostics of prostate cancer.


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