Characteristic features of carbazole phosphorescence quenching by benzophenone molecules in toluene at 77 K

We have studied the characteristic features of carbazole phosphorescence quenching by benzophenone in toluene at 77 K. We have shown that the decrease in the relative phosphorescence intensity for carbazole (energy donor) by a greater factor than we see for the relative change in its decay time is due to the fact that a change in the phosphorescence decay time occurs only for carbazole molecules participating in triplet-triplet energy transfer, while the substantial decrease in the phosphorescence intensity for carbazole with no change in the phosphorescence decay time is connected with quenching of its singlet states. __________ Translated from Zhurnal Prikladnoi Spektroskopii, Vol. 73, No. 4, pp. 554–556, July–August, 2006.     

三氟化硼引发四氢呋喃聚合的研究——Ⅳ.1,4-丁二醇的影响

前报中已证明用三氟化硼-环氧氯丙烷(ECH)引发四氢呋喃(THF)聚合具有较高的引发效率,并对在Ac_2O、水和无水存在下的聚合反应进行了研究。本文报道1,4-丁二醇(BG)对BF_3引发THF聚合反应的影响。通常认为在BG存在下,BF_3是不能引发THF聚合的,但本工作证明BG是有效的分子量调节剂,制备分子量在     

Theoretical analysis of dissociative adsorption of H2O on Ni(100)

In conclusion, let us note the principal results of the calculation.

以硫醚为主链的螯合树脂研究Ⅳ．含硫代硫酸根、叠氮基树脂的合成及吸附性能

聚环硫氯丙烷或环硫氯丙烷与环氧氯丙烷共聚物，在少量二乙烯三胺存在下制得交联预聚物，将交联预聚物分别与硫代硫酸钠，叠氮化钠反应，制得四种侧链带有硫代硫酸根或叠氮基的新型螯合树脂。它们对贵金属离子具有较高的吸附容量和较好的吸附选择性。     

Comparative structural characterization of the water dispersions of detonation nanodiamonds by small-angle neutron scattering

The structure of nanodiamond water dispersions prepared under different conditions was investigated by small-angle neutron scattering at the scale of 1 to 100 nm. The study of diluted dispersions was regarded as of paramount importance. Similarly to previous studies, strong clustering of particles was revealed in the solutions. The typical size of clusters (40 nm and above) depends on the modification of the dispersions. A common property can be distinguished for different systems: the fractal dimension of the clusters is in the range of 2.3?C2.4, which indicates that there is a common clustering mechanism in such systems. Using contrast variation, the existence of a nondiamond component in the colloidal particles of the dispersions was confirmed; it correlates with the presence of a graphene shell on crystallite surfaces.     

Structure of amyloid aggregates of lysozyme from small-angle X-ray scattering data

The structure of filament amyloid aggregates of hen egg white lysozyme in water has been investigated by the small-angle X-ray scattering method. The experimental data are described by different cylindrical models, among which the best agreement is reached with the long helix model. A comparison of the results with the small-angle neutron scattering data reveals the influence of the heavy component of the solvent (a H₂O/D₂O mixture) on the structure of the filaments.     

IN AQUA SYNTHESIS OF A HIGH MOLECULAR WEIGHT ARYLETHYNYLENE POLYMER EXHIBITING REVERSIBLE HYDROGEL PROPERTIES

ABSTRACT

A high molecular weight poly(aryleneethynylene) (M_w ～ 60,000) is prepared by the palladium catalyzed copolymerization of 3,5-diiodobenzoic acid and acetylene gas in a basic aqueous medium. The polymer has a “zig-zag”, fully conjugated backbone. The polymer has been characterized by a variety of methods and exhibits high thermal stability. Furthermore, the polymer is readily soluble in aqueous base and is reversibly switchable from the solution state to a hydrogel state, in water, by changing the pH of the solvent.     

Development of a general approach to the synthesis of a library of isoflavonoid derivatives

Isoflavonoids are a class of organic compounds that act primarily as antioxidants. They are produced almost exclusively by various members of the bean family including soybeans, tofu, peanuts, chick peas, and alfalfa. The antioxidant characteristics that isoflavonoids exhibit help hinder the progression of certain cancers, primarily breast, prostate, and colon cancer. We have developed a three-five step synthesis for obtaining a suite of isoflavonoid derivatives. The synthesis involves an enamine formation, a ring closure and halogenation, a Suzuki coupling, and finally a global deprotection to obtain the respective isoflavonoid derivatives.