A 3-D noninterpenetrating diamondoid network of a decanuclear copper(I) complex

The solvothermal reaction of CuCl(2).2H(2)O with pyridine-4-thiol and ethanol yielded a novel photoluminescent 3-D polymeric complex with an interesting decorated diamondoid network that is constructed of decanuclear copper(I) cluster units and mu(4)-Cl ligands. The in situ generation of CuSO(4).5H(2)O implies the spontaneous occurrence of desulfurization and redox reactions in the present system.     

Synthesis of fused polycyclic aromatics by palladium-catalyzed annulation of arynes using 2-halobiaryls

The Pd-catalyzed annulation of arynes by 2-halobiaryls and related vinylic halides provides a very efficient, high yielding synthesis of polycyclic aromatic and heteroaromatic hydrocarbons. This process appears to involve the catalytic, stepwise coupling of two very reactive substrates, an aryne and an organopalladium species, to generate excellent yields of cross-coupled products.     

The spin delocalization substituent parameter σ˙. 7. Meta-substituent effects on the cyclodimerization of trifluorostyrenes. A test for the σ˙JJ approach

Rate constants (k's) of the thermal cyclodimerization of ten meta-substituted trifluorostyrenes (m-Y-TFS's) have been measured in the temperature range 110–160°C. On the basis of these k's and the σ_mb values derived from ¹⁹F NMR data the spin-delocalization substituent constant σ^˙_m values of these ten meta-substituents have been calculated. The averaged σ^˙_m values are: m-Et, 0.09; m-t-Bu, 0.11; m-F, 0.03; m-Cl,?0.05; m-Br, 0.12: m-CF₃, ?0.07; m-OMe, 0.10; m-NO₂, ?0.002; m-CN, 0.11 and m-CO₂Me, 0.08. Both the smallness of these values and the nonexistence of correlation between Hammett-Type polar σ^X and these σ^˙_m values support our belief that the σ_j?J approach is reliable and trustworthy.     

甲烷在Mo/HZSM-5催化剂上的脱氢聚合反应

对不同Mo含量的Mo／HZSM－5催化剂的结构进行了表征，并对这些催化剂的甲烷非氧气氛下的转化反应进行了考察．催化剂的BET比表面积及酸性随Mo含量的增加而降低，当Mo含量大于5％时，Mo对ZSM－5分子筛的晶型有影响，并出现MoO3物相．甲烷在700℃时可高选择性地生成苯和乙烯，最佳Mo含量大约为2％．纯的MoO3或HZSM－5上该反应几乎不进行，因此，可能是分散的钼氧离子和分子筛的酸中心是甲烷转化的活性中心，只有二者的协同作用才能促进甲烷的转化．反应后催化剂中的钼物种被还原了．催化剂上的积炭可能是催化剂失活的主要原因之一，烧炭后催化剂活性基本恢复．     

Reentrant behavior of poly(N-isopropylacrylamide) brushes in water-methanol mixtures investigated with a quartz crystal microbalance

The solvent composition induced reentrant behavior of poly(N-isopropylacrylamide) (PNIPAM) chains grafted on a SiO2 surface in water-methanol mixtures was investigated using a quartz crystal microbalance with dissipation monitoring (QCM-D) at 20 degrees C. The frequency and energy dissipation responses showed that the grafted PNIPAM chains sharply collapse when the methanol content (x(m)) reaches approximately 17 mol %. In the range 17-50 mol %, the grafted chains remain in a collapsed state. Further increase of the methanol content leads to an abrupt reswelling of the collapsed chains at x(m) > approximately 50 mol %. The sharp reentrant swelling-to-collapse-to-swelling transition was attributed to the water-methanol complexation instead of the preferential adsorption effect. Our results also suggest that the water-methanol complexation is not induced by hydrophobic interaction but by hydrogen bonding.     

Growth of porous single-crystal Cr2O3 in a 3-D mesopore system

Single-crystal Cr2O3 with regular mesopores has been synthesized using mesoporous silica KIT-6 as a template and characterized by using XRD, HRTEM and nitrogen adsorption/desorption.     

A practical synthesis of 2-(N-substituted)-aminobenzimidazoles utilizing CuCl-promoted intramolecular cyclization of N-(2-aminoaryl)thioureas

A practical protocol for synthesis of 2-(N-substituted)-aminobenzimidazoles was developed. N-(2-Aminoaryl)thioureas undergo a CuCl-promoted intramolecular cyclization to give the corresponding 2-(N-substituted amino)benzimidazoles in good to excellent isolated yields.     

液-液萃取电感耦合等离子体质谱法测定天然水中痕量稀土元素

建立了以单、二（2－乙基己基）磷酸酯混合螯合剂的庚烷溶液作为萃取剂，6.0mol/L HCl反萃取预分离富集，In和Rh做内,ICP-MS测定天然水中15种稀土元素的分析方法。方法的富集倍数为200倍，各元素的检出限范围在0.01-1.8ng/L之间，相对标准偏差RSD＜5％，萃取回收率＞93％。     

Order from Chaos: Self‐Assembly of Nanoprism from a Mixture of Tetratopic Terpyridine‐Porphyrin Conformers

Porphyrins have been widely used in the self‐assembly of metallo‐supramolecules. In this study, we introduced 2,2':6,2"‐terpyridine (tpy) into a porphyrin core to synthesize a tetratopic building block with multiple conformers. During the self‐assembly with Zn(II), such a mixture of conformers was able to form a discrete nanoprism with all building blocks in one conformation. Detailed characterizations, including NMR, ESI‐MS and traveling‐wave ion mobility‐mass spectrometry (TWIM‐MS), all supported the formation of the desired assemblies. AFM and TEM further confirmed the dimensions of assembled nanoprisms. Moreover, the photophysical properties of the ligands and complexes were noticeably different depending upon size and metal ion center.     

Hosoya polynomials of armchair open‐ended nanotubes

For a connected graph G we denote by d(G,k) the number of vertex pairs at distance k. The Hosoya polynomial of G is H(G,x) = ∑_k≥0 d(G,k)x^k. In this paper, analytical formulae for calculating the polynomials of armchair open‐ended nanotubes are given. Furthermore, the Wiener index, derived from the first derivative of the Hosoya polynomial in x = 1, and the hyper‐Wiener index, from one‐half of the second derivative of the Hosoya polynomial multiplied by x in x = 1, can be calculated. © 2006 Wiley Periodicals, Inc. Int J Quantum Chem, 2007