Synthesis of a bifunctional boron-Lewis acid and studies on host-guest chemistry using pyridine and TMPD

Based on the previously described bifunctional Lewis acid with a functional distance of the boron functions of 4.918(2) Å, the development of a further bifunctional, boron-containing Lewis acid with a wider functional distance is demonstrated. Again, a stannylated precursor was used and the Lewis-acidic boron functions were introduced by means of tin-boron exchange. The general suitability of this class of compounds for the formation of host-guest-complexes is demonstrated by NMR experiments and by solid-state structures using pyridine and TMPD (N 1,N 1,N 4,N 4-tetramethylbenzene-1,4-diamine) as Lewis basic guests. The influence of traces of moisture on the boron-containing, bifunctional Lewis acids was investigated by the structure elucidation of a decomposition product.

Synthetic and Structural Study of peri-Substituted Phosphine-Arsines

A series of phosphorus-arsenic peri-substituted acenaphthene species have been isolated and fully characterised, including single crystal X-ray diffraction. Reactions of EBr3 (E = P, As) with iPr2PAcenapLi (Acenap = acenaphthene-5,6-diyl) afforded the thermally stable peri-substitution supported donor–acceptor complexes, iPr2PAcenapEBr23 and 4. Both complexes show a strong P→E dative interaction, as observed by X-ray crystallography and 31P NMR spectroscopy. DFT calculations indicated the unusual As∙∙∙As contact (3.50 Å) observed in the solid state structure of 4 results from dispersion forces rather than metallic interactions. Incorporation of the excess AsBr3 in the crystal structure of 3 promotes the formation of the ion separated species [iPr2PAcenapAsBr]+Br− 5. A decomposition product 6 containing the rare [As6Br8]2– heterocubane dianion was isolated and characterised crystallographically. The reaction between iPr2PAcenapLi and EtAsI2 afforded tertiary arsine (BrAcenap)2AsEt 7, which was subsequently lithiated and reacted with PhPCl2 and Ph2PCl to afford cyclic PhP(Acenap)2AsEt 8 and acyclic EtAs(AcenapPPh2)2 9.

Decarboxylation of p-Coumaric Acid during Pyrolysis on the Nanoceria Surface

Temperature-programmed desorption mass spectrometry (TPD MS) was used to study the pyrolysis of p-coumaric acid (pCmA) on the nanoceria surface. The interaction of pCmA with the CeO2 surface was investigated by FT-IR spectroscopy. The obtained data indicated the formation on the nanoceria surface of bidentate carboxylate complexes with chelate (Δν = 62 cm−1) and bridge structure (Δν = 146 cm−1). The thermal decomposition of pCmA over nanoceria occurred in several stages, mainly by decarboxylation. The main decomposition product is 4-vinylphenol (m/z 120). The obtained data can be useful for studying the mechanisms of catalytic thermal transformations of lignin-containing raw materials using catalysts containing cerium oxide and the development of effective technologies for the isolation of pCmA from lignin.

Analysis of Suspended Potential Discharge Defects by SF6 Decomposition Products

The type and content of SF6 decomposition products are directly related to the type, location and degree of fault. Based on the analysis of the abnormal SF6 gas decomposition product content and discharge type of 126kV Porcelain Column type circuit breaker, the potential fault of the circuit breaker is judged to be suspension potential discharge fault. After disassembling the circuit breaker, it is found that the abnormal phase of the insulation rod is deformed, the pin become thin, and there are solid decomposition products, the sulfides and fluoride, which are mainly composed of iron, aluminum, chromium and manganese, further confirm that the potential fault of the circuit breaker is suspension potential discharge fault. The forming process and reaction mechanism of the suspended potential discharge fault are analyzed. Once the fault occurs, its function will promote the development of the fault. The influence of the suspension potential discharge fault on the performance of the circuit breaker is also analyzed. When the suspension potential discharge fault exists, it will cause the abnormality and even affect the normal operation of the circuit breake.

The Effect of Additive Chemical Structure on the Tribofilms Derived from Varying Molybdenum-Sulfur Chemistries

Molybdenum disulfide (MoS2) is an effective friction modifier that can be formed on surfaces from oil-soluble lubricant additives. Different additive chemistries can be used to form MoS2 on a surface. The tribofilms formed from three different molybdenum additives (MoDTC Dimer, MoDTC Trimer, and molybdate ester) were studied in additive monoblends and fully formulated systems. The resulting tribofilms were then characterized by Raman spectroscopic spatial mapping, XPS, and FIB-TEM. The distribution of MoS2 on the surface was much more sparse for the molybdate ester than the other additives. No crystalline molybdenum oxides were observed by Raman spectroscopy, but their presence was inferred from XPS analysis. XPS analysis showed very similar distributions of Mo oxidation states from each additive, such that the chemical nature of the films formed from all of the additives is likely similar. Each of the additive tribofilms was observed to have MoS3 vibrations in Raman and persulfide XPS peaks associated with amorphous MoS3, as such this species is presented as a common frictional decomposition product for all the additives. The MoDTC trimer is more able to produce this amorphous species on the contacting surfaces due to its structural similarities to the co-ordination polymer MoS3. Graphical Abstract

Oral Microbial Diversity Formed and Maintained through Decomposition Product Feedback Regulation and Delayed Responses

Oral microbial diversity plays an important role on oral health maintenance. However, there are only few kinds of substrates available for the microbial flora in oral cavity, and it still remains unclear why oral microbial diversity can be formed and sustained without obvious competitive exclusion. Based on experimental phenomena and data, a new hypothesis was proposed, namely, the decomposition product negative feedback regulation on microbial population size and microbial delay responses including reproductive, reaction, interspecific competition, and substrate decomposition delay responses induced by oral immunity. According to hypothesis and its cellular automata (CA) model, the CA simulation results sufficiently proved that the decomposition product negative feedback regulation and four microbial delay responses could significantly alleviate the interspecific competitions and inhibit the emergence of dominant species, causing the formation and sustenance of oral microbial diversity. This study could also offer effective guidance of prevention and treatment of oral cavity diseases.