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T Sierra

Publications and source records attributed to T Sierra.

7 recordsLinked to original sources
PubMed2001

The 1,2,4-triazolyl cation: thermolytic and photolytic studies.

The generation of the 1,2,4-triazolyl cation (1) has been attempted by the thermolysis and photolysis of 1-(1,2,4-triazol-4-yl)-2,4,6-trimethylpyridinium tetrafluoroborate (2) and the thermolysis of 1- and 4-diazonium-1,2,4-triazoles, using mainly mesitylene as the trapping agent. Thermolysis of 2 gave mostly 1,2,4-triazole, together with 3-(1,2,4-triazol-4-yl)-2,4,6-trimethylpyridine, 4-(1,2,4-triazol-4-ylmethyl)-2,6-dimethylpyridine, and 4-(2,4,6-trimethylbenzyl)-2,6-dimethylpyridine. Thermolysis of each of the diazonium salts in the presence of mesitylene again gave mainly triazole together with very low yields of 1-(1,2,4-triazol-1-yl)-2,4,6-trimethylbenzene and the corresponding -4-yl isomer in about the same ratio. On the other hand, photolysis of 2 in mesitylene gave mainly 1-(1,2,4-triazol-1-yl)-2,4,6-trimethylbenzene. A photoinduced electron transfer from mesitylene to 2 has been observed and preliminary laser flash photolyses of 2 and the corresponding 2,4,6-triphenylpyridinium salt have been carried out. The observed transients are explained as arising from the first excited states of the pyridinium salts rather than from 1. Ab initio MO calculations are reported and indicate that the predicted electronic ground-state of the triazolyl cation is a triplet state of B1 symmetry with five pi electrons, which corresponds to a diradical cation (1c). Possible mechanisms for the formation of the various products are proposed.

Journal Article↗
PubMed2000

Switchable columnar metallomesogens

Chiral columnar liquid crystals have recently appeared as a promising new type of ferroelectric materials. To date, all the columnar liquid crystals that have been reported to show ferroelectric switching consist of organic compounds. However, metal-containing liquid crystals open this field to a significant number of new structures and offer the possibility of adding to the ferroelectric behavior other properties inherent to the presence of metals in the structure, such as magnetism, as well as the use of new methods of characterization (EPR, synchrotron radiation, etc.). The potential of columnar metal-containing liquid crystals as ferroelectric materials has been demonstrated even though only a few organic columnar ferroelectric liquid crystals have been described. As a first approach to this type of material, this concepts article describes the results obtained with chiral metal beta-diketonates that show ferroelectric switching in the columnar mesophase. It has been shown that these materials have a helical columnar arrangement in the mesomorphic state, and a chiral superstructure has been proposed from circular dichroism studies. This type of supramolecular structure plays a fundamental role in the ferroelectric properties of these compounds. The discussion is mainly focused on the strategy employed for the molecular design, and on the interpretation of the mesophase structure and the electrooptic effect. The use of a diverse range of techniques, both those commonly used in the field of liquid crystals and those that are more specific will be highlighted, and the principles of these specific techniques are summarized together with a justification of their applicability to this study.

Journal Article↗
PubMed1998

The PA influenza virus polymerase subunit is a phosphorylated protein.

The induction of proteolysis by expression of the influenza virus PA polymerase subunit is the only biochemical activity ascribed to this protein. In the course of studying viral protein synthesis by two-dimensional gel electrophoresis, we observed the existence of several PA isoforms with different isoelectric points. These isoforms were also present when the PA gene was singly expressed in three different expression systems, indicating that a cellular activity is responsible for its post-translational modification. In vivo labelling with [32P]orthophosphate, followed by two-dimensional gel electrophoresis, clearly demonstrated the incorporation of phosphate into the PA molecule. Phosphoserine and phosphothreonine epitopes were present in PA, while phosphotyrosine residues were absent, as tested by immunoblotting with specific antibodies. These facts, as well as the presence of multiple consensus sites for casein kinase II (CKII) phosphorylation, prompted us to test the involvement of this kinase in PA covalent modification. PA protein purified by immunoprecipitation could be specifically labelled by the catalytic alpha subunit of human CKII, which was expressed and purified from bacteria. Collectively, these data demonstrate that the PA subunit of the influenza virus RNA polymerase is a phosphoprotein.

Animals↗