NIR and UV induced transformations of indazole-3-carboxylic acid isolated in low temperature matrices.

The molecular structure and NIR and UV induced phototransformations of indazole-3-carboxylic acid were studied in low temperature argon and nitrogen matrices by FTIR spectroscopy and B3LYP/6-311++G(2d,2p) calculations. Eleven minima of IC were located on the S0 potential energy surface. The three most stable structures were detected experimentally in both matrices after deposition. Upon NIR irradiation a dominant process was rotamerization within the carboxylic group leading to changes in the population of the trans 1HIC1 and cis 1HIC2 forms. In turn, at UV irradiation at λ = 260 nm two new tautomers (2HIC2 and 2HIC3) were generated indicating that the hydrogen atom transfer in pyrazole ring took place. Based on the obtained kinetic curves, differences in the phototransformation rates in different matrices were indicated.

Structure and IR spectroscopic properties of complexes of 1,2,4-triazole and 3-amino-1,2,4-triazole with dinitrogen isolated in solid argon.

Complexes of 1,2,4-triazole (TR) and 3-amino-1,2,4-triazole (AT) with N2 were studied computationally employing MP2 and B3LYPD3 methods and experimentally by FTIR matrix isolation technique. The results show that both triazoles interact specifically with dinitrogen in several different ways. For the 1:1 complexes of 1,2,4-triazole five stable minima were located on the potential energy surface. The most stable of them comprises a weak hydrogen bond formed between the NH group of the ring and the lone pair of the nitrogen molecule. The second most stable structure is bound by the N⋯π bond formed between one of the N atoms of the N2 molecule and the triazole ring. Three other complexes are stabilized by the C-H⋯N and N⋯N van der Waals interactions. In the case of 3-amino-1,2,4-triazole, the two most stable dinitrogen complexes are analogous to those found for the 1,2,4-triazole and involve N-H⋯N and N⋯π bonds. In other structures amino or CH groups act as proton donors to the N2 molecule. The N⋯N van der Waals interactions are also present. The analysis of the infrared spectra of low temperature matrices containing TR or AT and dinitrogen indicates that in both systems mostly 1:1 hydrogen-bonded complexes with the NH group interacting with N2 are present in solid argon.

FTIR spectroscopic evidence for new isomers of 3-aminopyrazine-2-carboxylic acid formed in argon matrices upon UV irradiations.

The UV-induced photochemistry and molecular structure of 3-aminopyrazine-2-carboxylic acid were studied in argon matrices by Fourier-transform infrared spectroscopy and B3LYP/6-311++G(2d,2p) calculations. Out of seventeen possible isomers of this molecule located on the singlet potential energy surface the most stable one, APA1 comprising intramolecular O-H···N and N-H···O hydrogen bonds, was detected experimentally in the matrix after deposition. Two new conformers APA2 and APA3 were generated upon irradiation with λ = 280 nm by trans/cis-COOH isomerization and at λ = 360 nm by COOH group rotamerization, respectively, whereas an amino-imino tautomerization leading to IPA1 and IPA2 structures occurred at λ = 305 nm. The reverse reactions were also observed upon irradiation of the matrices at 265, 230 and 400 nm. Simultaneously with the photoisomerizations, a cleavage of the pyrazine ring along with CO2 elimination was observed leading to the formation of carbodiimide and cyanamide derivatives.

Phototransformations of 2-(1,2,4-Triazol-3-yl)benzoic Acid in Low Temperature Matrices.

Phototransformations of 2-(1,2,4-triazol-3-yl)benzoic acid induced by tunable UV laser were studied in low temperature matrices by FTIR spectroscopy. Out of 36 possible isomers of this molecule the most stable one, comprising the intramolecular N-H···O hydrogen bond, was detected experimentally in argon and xenon matrices after deposition. Upon irradiation with λ = 325 nm, two new conformers of the precursor were formed. The corresponding reverse photorotamerizations were also detected at 250 nm partly reproducing the initial molecules. In addition to the conformational changes, an interesting photoisomerization took place in the studied matrices leading to a proton transfer from N atom of the triazole ring to the carbonyl oxygen of the carboxylic group. As a result of this reaction, a new product with two OH groups was identified for the first time. The experimental studies were supported by DFT calculations in both ground and excited electronic states.

Carboxylic group and its tetrazolyl isostere in one molecule. Matrix isolation FTIR and DFT studies on thermal decomposition and photochemistry of (tetrazol-5-yl)acetic acid.

The title compound (tetrazol-5-yl)acetic acid (TA) is an interesting molecule that contains both a carboxylic group and its isostere tetrazolyl group. Out of nine theoretically predicted stable structures of TA, three appeared to be present in solid argon. Thermal decomposition of the species aided by water molecules was studied in detail both experimentally using FTIR matrix isolation technique and theoretically at the B3LYP/6-311++G(2d,2p) level. Experimentally, it was found that the decarboxylation process appeared at the presence of water traces in the system. Theoretically, it was shown that the energy barrier of the water assisted process was lower by ca. 30 kJ mol(-1) comparing to the process without water participation. The UV photolysis of the TA/Ar system was studied using both broad-band and narrow-band sources. The main photoproducts appeared to be carbodiimidylacetic acid and (1H-diaziren-3-yl)acetic acid. The progress of the reactions induced was followed by FTIR spectroscopy, whereas interpretation of the results was supported by quantum chemical calculations (DFT, TD-DFT).

Infrared spectra and X-ray structure of (tetrazol-5-yl)acetic acid.

The (tetrazol-5-yl)acetic acid crystal was characterized by the X-ray diffraction and FTIR spectroscopic methods. The analysis of the crystal structure reveals that the compound exists in the solid state as 1H-tautomer. The molecules are linked by two types of the intermolecular hydrogen bonds forming an infinite two-dimensional network in the (101) plane. Intramolecular N-H···O hydrogen bonds are also formed in the crystal. The analysis of the FTIR spectra of the crystalline sample and its deuterated analogue, based on the B3LYP/6-311++G(2d,2p) frequency calculations of two model tetramers, has been performed in relation to the obtained crystal structure data.

Conformational behavior and tautomer selective photochemistry in low temperature matrices: the case of 5-(1H-tetrazol-1-yl)-1,2,4-triazole.

The conformational properties and the photolysis behavior of one of the simplest N-C bonded bicyclic azoles, 5-(1H-tetrazol-1-yl)-1,2,4-triazole (T), were studied in argon and xenon matrices by infrared spectroscopy. Analysis of the experimental results was supported by extensive theoretical calculations carried out at the B3LYP/6-311++G(2d,2p) level of approximation. Out of the eight T minima located on the potential energy surface, the three most stable species were detected in low temperature matrices, namely, 5-(1H-tetrazol-1-yl)-1H-1,2,4-triazole (T1) and two conformers of 5-(1H-tetrazol-1-yl)-2H-1,2,4-triazole (T2a and T2b). With increase of the substrate temperature either during deposition of the matrices or during annealing the T2b → T2a conversion took place, in agreement with the predicted low energy barrier for this transformation (5.38 kJ mol(-1)). Both broad band and narrow band laser UV irradiations of T isolated in Xe and Ar matrices induce unimolecular decomposition involving cleavage of the tetrazole ring of T1 and T2a (T2b) that leads to the production of 1H-1,2,4-triazol-5-yl carbodiimide (P1) and 1H-1,2,4-triazol-3-yl carbodiimide (P2), respectively. When the laser is used, in addition to the main P1 and P2 photoproducts, several minor products could be successfully identified in the matrices: N-cyanocarbodiimide HNCNCN (detected for the first time) associated with nitrilimine HNNCH and HCN. An interesting phenomenon of tautomer-selective photochemistry was observed for the matrix-isolated compound. It could be explained by the different LUMO-HOMO energy gaps estimated for T1, T2a, and T2b, connected with different threshold energies necessary to start the photolysis of T1 and T2a (T2b).