Quantification of microbial community assembly processes during degradation on diverse plastispheres based on physicochemical characters and phylogenetic bin-based null model analysis.

To understand the differences in degradation processes depending on the chemical properties of polymers, it is necessary to both quantify the microbiome composition and evaluate the process of microbial turnover (i.e., community assembly processes) in a variety of polymer materials.

Encouragements for the Use of Microwaves in Industrial Chemistry.

Microwave travels at the speed of light, and transfers energy solely to materials. This holds great promise for energy conservation in industrial processes. However, due to differences with common heating principles, and misunderstanding of the correct way to handle them, the effectiveness of microwaves has been underestimated, and development of technologies using microwaves often stops due to this.

A new oxapalladacycle generated via ortho C-H activation of phenylphosphinic acid: an efficient catalyst for Markovnikov-type additions of E-H bonds to alkynes.

A new oxapalladacycle 3 can be conveniently prepared via direct ortho palladation of diphenylphosphinic acid with palladium acetate. Catalysts derived from 3 can efficiently catalyze Markovnikov-type additions of E-H bonds (P(O)-H, S-H and spC-H) to alkynes via a unique catalytic cycle.

Enhancement of the large stokes-shifted fluorescence emission from the 2-(2'-hydroxyphenyl)benzoxazole core in a dendrimer.

The photochemical properties of a series of newly synthesized dendrimers, 4-6, having a 2-(2'-hydroxyphenyl)benzoxazole (HBO) core, were studied in benzene. The fluorescence quantum yields (Phi(f)) were determined to be 0.022, 0.

Photoisomerisation and fluorescence behaviour of polyphenylene-based stilbene dendrimers.

The photoinduced structural changes of three polyphenylene-based stilbene dendrimers, G1, G2, and G3, has been studied. They all exhibit fluorescence emission with considerably higher quantum efficiency and longer fluorescence lifetimes compared with the parent stilbene. These dendrimers undergo mutual cis --> trans isomerisation on direct irradiation with 310 nm light at room temperature.

Evaluation of the quantitativeness of matrix-assisted laser desorption/ionization time-of-flight mass spectrometry using an equimolar mixture of uniform poly(ethylene glycol) oligomers.

Quantitativeness of matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOFMS) was elucidated using an equimolar mixture of uniform poly(ethylene glycol) (PEG) oligomers with no molecular weight distributions. Uniform PEG oligomers with degrees of polymerization n = 6-40 were separated from commercial PEG samples by preparative super-critical fluid chromatography. MALDI-TOF mass spectra of an equimolar mixture of the uniform PEG oligomers were recorded by adding a mixture of 2,5-dihydroxybenzoic acid as a matrix reagent and four chlorinated salts, i.

Photoisomerization of stilbene dendrimers: the need for a volume-conserving isomerization mechanisms.

Highly branched stilbene dendrimers were synthesized and their photochemical behavior was studied. Even the stilbene dendrimer with molecular weight over 6500 underwent trans-cis isomerization in the excited singlet state within the lifetime of 10 ns. The photoisomerization of C=C double bond of stilbene dendrimers in the excited state may proceed by a volume-conserving novel mechanism such as hula-twist rather than conventional 180 degrees rotation around the C=C double bond based on fluorescence and isomerization experiments.