On the photofragmentation of SF2+_2^+: Experimental evidence for a predissociation channel

We report on the first observation of the photofragmentation dynamics of SF$_2^+$. With the aid of state-of-the-art ab initio calculations on the low-lying excited cationic states of SF$_2^+$ performed by Lee et al. [J. Chem. Phys. 125, 104304 (2006)], a predissociation channel of SF$_2^+$ is evidenced by means of resonance-enhanced multilphoton ionization spectroscopy. This work represents a second experimental investigation on the low-lying excited cationic states of SF$_2^+$. [The first one is the He I photoelectron spectrum of SF$_2^+$ reported by de Leeuw et al. three decades ago, see Chem. Phys. 34, 287 (1978).]Comment: 7 pages, 3 figures, submitted to JCP as a Not

Reactions of C2_2({\it a}3Piu^3Pi_u) with selected saturated alkanes: A temperature dependence study

We present a temperature dependence study on the gas phase reactions of the C$_2$({\it a}$^3Pi_u$) radical with a selected series of saturated alkanes (C$_2$H$_6$, C$_3$H$_8$, n-C$_4$H$_10$, i-C$_4$H$_10$, and n-C$_6$H$_14$) by means of pulsed laser photolysis/laser-induced fluorescence technique. The bimolecular rate constants for these reactions were obtained between 298 and 673 K. A pronounced negative temperature effect was observed for n-C$_4$H$_10$, i-C$_4$H$_10$, and n-C$_6$H$_14$ and interpreted in terms of steric hindrance of the more reactive secondary or tertiary C-H bonds by less reactive CH$_3$ groups. Detailed analysis of our experimental results reveals quantitatively the temperature dependence of reactivities for the primary, secondary, and tertiary C-H bonds in these saturated alkanes and further lends support to a mechanism of hydrogen abstraction.Comment: 26 pages, 8 figures, 1 table, 30 references; accepted to JC

Poly[tris­(μ-benzene-1,4-dicarboxylato)bis­(dipyrido[3,2-a:2′,3′-c]phenazine)trimanganese(II)]

In the title compound, [Mn3(C8H4O4)3(C14H8N4)2]n, one Mn atom is located on an inversion centre and is six-coordinated by four carboxyl­ate O atoms from different benzene-1,4-dicarboxyl­ate (1,4-bdc) ligands and two phenanthrene N atoms from a dipyrido[3,2-a:2′,3′-c]phenazine ligand. The other Mn atom is also six-coordinate, binding to six carboxyl­ate O atoms from different 1,4-bdc ligands. The dicarboxyl­ate groups chelate and bridge the two Mn atoms and a symmetry-related Mn atom to form a trimanganese unit. Bridging of the trinuclear MnII clusters leads to a two-dimensional structure

Biomass-derived three-dimensional porous N-doped carbonaceous aerogel for efficient supercapacitor electrodes

Functionalized carbonaceous materials with hierarchical structure and developed porosity are highly desired in energy storage and conversion fields. In this work, a facile and scalable hydrothermal methodology was established to synthesise three-dimensional (3D) N-doped carbonaceous aerogels using biomass-based starting materials and polypyrrole as N-source. The effect of different calcination temperatures on the structural properties, type and content of N-species and electrochemical performance of the 3D N-doped carbonaceous aerogels were uncovered. Thanks to the combinatorial effect of the appropriate N content and porous structure, the obtained samples exhibited excellent electrochemical performance, in particular, an outstanding specific capacitance of 281.0 F g-1 achieved on the sample calcined at 600 °C. This methodology offers a new fabrication strategy to prepare nanoscale carbonaceous materials with desirable morphology and hierarchical architecture of great potentials for the applications in energy fields