Symmetry operators of generalized wreath products and their applications to chemical physics

Symmetry operators of generalized wreath product groups are formulated. Several applications of these operators to nonrigid molecular problems in chemical physics are outlined.     

Solid-phase synthesis of N-alkyl-N-(beta-keto)amides and 1,2,4,5-tetrasubstituted imidazoles using a traceless cleavage strategy

[reaction: see text] The solid-phase synthesis of N-alkyl-beta-keto)amides and 1,2,4,5-tetrasubstituted imidazoles was demonstrated using a traceless cleavage strategy based on benzylic acylammonium chloride reactivity. The approach enables the assembly of diverse compounds in a minimal number of steps in moderate to excellent yield (23-88%) and high purity (64-100%).     

Site-specific cleavage of human telomerase RNA using PNA-neocuproine.Zn(II) derivatives

Here we report the synthesis of a novel PNA based neocuproine.Zn RNA cleaving agent; we demonstrate that such agents sequence specifically cleave a synthetic RNA target and in particular the RNA component of human telomerase.     

On the claisen rearrangement of 1,4-diaryloxy-2-butynes

A proton nmr follow-up provided conclusive evidence for the involvement of two sequential Claisen rearrangements in the thermal rearrangement of 1,4-diaryloxy-2-butynes $\text{1}$to 11a-methylpterocarpans $\text{3}$. A detailed study of the rearrangement of 1,4-diaryloxy-2-butynes $\text{1}$ in polyethyleneglycol-200 (PEG-200), indicated a definite possibility of selective synthesis of either benzofuron (3,2-b )benzofuran $\text{4}$ or benzofuro(2,3-b)benzofuran $\text{5}$ by varying the temperature of the reaction alone     

Computer generation of edge groups and edge colorings of graphs

A computer code and nonnumerical algorithm are developed to construct the edge group of a graph and to enumerate the edge colorings of graphs of chemical interest. The edge colorings of graphs have many applications in nuclear magnetic resonance (NMR), multiple quantum NMR, enumeration of structural isomers of unsaturated organic compounds, and in the construction of configurational integral expansion series in statistical mechanics. The code developed is applied to many NMR graphs, complete graphs containing up to 10 vertices, and the Petersen graph.     

Spectrophotometric determination of the stability constants of HgCl(-)3 and HgCl(2-)4 in aqueous ethanol

The stability constants of HgCl(-)(3) and HgCl(2-)(4) in 60% aqueous ethanol (v/v) were determined by spectroscopy at 25 degrees and constant ionic strength and acidity; beta(1) was 3 +/- 1 and beta(2) 9 +/-3.     

On the maximal length of two sequences of integers in arithmetic progressions with the same prime divisors

In this paper we consider an analogue of the problem of Erds and Woods for arithmetic progressions. A positive answer follows from theabc conjecture. Partial results are obtained unconditionally.     

Microenvironmental differences amongst micelles of various shapes and structures

Micelles of different amphiphiles adopt different shapes and internal packing arrangements in water, depending on their chemical structures and the conditions of the medium. Two microenvironmental features, namely the polarity and the microviscosity that the aggregate offers to a solubilized molecule, have been monitored using extrinsic fluorescence probes. While the differences between micelles of spherical and rod-like shapes are not always distinct, stacked micelles and peptide micelles offer distinctly lower polarity and higher microviscosity to solubilizates than the others.     

Photochemical and thermal transformations of 7-silabicyclo[2.2.1]Heptadiene and 7-silabicyclo[2.2.1]heptene systems

2,3-Dicarbomethoxy-7,7-dimethyl-7-silabicyclo[2.2.1]hepta-2,5-diene (III) on photolysis gave dimethyl tetraphenylphthalate whereas the photolysis of 7,7-dimethyl-7-silabicyclo[2.2.1]hep-5-ene-2,3-dicarboxylic anhydride (XIa) resulted in the formation of 1,1-dimethyl-2,3,4,5-tetraphenyl-1-silacyclopentadiene (XIIIa). The thermolysis of XIa also gave rise to XIIIa. Similarly, the photolysis as well as thermolysis of 1,4,5,6,7,7-hexaphenyl-7-silabicyclo[2.2.1]hept-5-ene-2,3-dicarboxylic anhydride (XIb) led to hexaphenylsilacyclopentadiene (XIIIb). Attempts to detect radical intermediates in these thermal and photochemical transformations by carrying out the reaction in the presence of hydroquinone, hydrazobenzene, 3,6-diphenyl-1,2-dihydro-1,2,4,5-tetrazine, cumene and tolan were unsuccessful. An attempted preparation of 7-silabicyclo[2.2.1]hepta2,5-dienes by the reaction of silacyclopentadienes such as 1-methyl-1-vinyl2,3,4,5-tetraphenyl-1-silacyclopentadiene (XV) and 1-methyl-1,2,3,4,5-pentaphenyl-1-silacyclopentadiene (XVI) with dimethyl acetylenedicarboxylate resulted in the isolation of dimethyl tetraphenylphthalate indicating that the corresponding 7-silabicyclo[2.2.1]hepta-2,5-dienes are thermally unstable.     

Symmetry allowed π4s+π2s additions silacyclopentadienes

π⁴s+π²s cycloaddition of hexaphenylsilacyclopentadiene with ethyl acrylate gives rise to a bicyclosilaheptene derivative. High resolution NMR studies have shown that the ester group in this adduct is in the endo position and that the ester methylene protons are magnetically inequivalent. Similar cycloadditions of hexaphenylsilacyclopentadiene, 1,1-dimethyl-2,3,4,5-tetraphenylsilacyclopentadiene, 1-methyl-1,2,3,4,5-pentaphenylsilacyclopentadiene, and 1-methyl-1-vinyl-2,3,4,5-tetra-phenylsilacyclopentadiene with dienophiles like acrylonitrile, maleic anhydride and dibenzoylacetylene have been carried out. The stereochemistry of these adducts has been deduced on the basis of NMR studies. Mass spectral fragmentation studies of some of the silabicycloheptenes have been carried out.