Theoretical study on the mechanism of extraction reaction between silylene carbene and its derivatives and thiirane

The mechanism of the sulfur extraction reaction between singlet silylene carbine and its derivatives and thiirane has been investigated with density functional theory (DFT), including geometry optimization and vibrational analysis for the involved stationary points on the potential energy surface. The energies of the different conformations are calculated by B3LYP/6-311G(d, p) method. From the potential energy profile, it can be predicted that the reaction pathway of this kind consists in two steps: (1) the two reactants firstly form an intermediate through a barrier-free exothermic reaction; (2) the intermediate then isomerizes to a product via a transition state. This kind of reactions has similar mechanism: when the silylene carbene and its derivatives [X₂Si=C: (X = H, F, Cl, CH₃)] and thiirane approach each other, the shift of 3p lone electron pair of S in thiirane to the 2p unoccupied orbital of C in X₂Si=C: gives a p → p donor-acceptor bond, thereby leading to the formation of intermediate (INT). As the p → p donor-acceptor bond continues to strengthen (that is the C-S bond continues to shorten), the intermediate (INT) generates product (P + C₂H₄) via transition state (TS). It is the substituent electronegativity that mainly affect the extraction reactions. When the substituent electronegativity is greater, the energy barrier is lower, and the reaction rate is greater.     

Coordination networks from Cu cations and tetrakis(methylthio)benzenedicarboxylic acid: tunable bonding patterns and selective sensing for NH(3) gas

This paper aims to illustrate the rich potential of the thioether-carboxyl combination in generating coordination networks with tunable and interesting structural features. By simply varying the ratio between Cu(NO(3))(2) and the bifunctional ligand tetrakis(methylthio)benzenedicarboxylic acid (TMBD) as the reactants, three coordination networks can be hydrothermally synthesized in substantial yields, which present a distinct evolution with regard to metal-ligand interactions. Specifically, Cu(TMBD)(0.5)(H(2)TMBD)(0.5)·H(2)TMBD (1) was obtained with a relatively small (1:1) Cu(NO(3))(2)/TMBD ratio, and crystallizes as an one-dimensional (1D) coordination assembly based on Cu(I)-thioether interactions, which is integrated by hydrogen-bonding to additional H(2)TMBD molecules to form a three-dimensional (3D) composite network with all the carboxylic acid and carboxylate groups remaining uncoordinated to the metal ions. A medium (1.25:1) Cu(NO(3))(2)/TMBD ratio leads to compound Cu(2)TMBD, in which Cu(I) ions simultaneously bond to the carboxylate and thioether groups, while an even higher (2.4:1) Cu(NO(3))(2)/TMBD ratio produced a mixed-cation compound Cu(II)(2)OHCu(I)(TMBD)(2)·2H(2)O (2), in which the carboxylic groups are bonded to (cupric) Cu(II) ions, and the thioether groups to Cu(I). Despite the lack of open channels in 2, crystallites of this compound exhibit a distinct and selective absorption of NH(3), with a concomitant color change from green to blue, indicating substantial network flexibility and dynamics with regards to gas transport.     

Theoretical study of mechanism of cycloaddition reaction between dimethylmethylene carbene and formaldehyde

The cycloaddition mechanism of forming a polycyclic compound between singlet dimethylmethylene carbene(R1) and formaldehyde(R2) has been investigated with MP2/6‐31G* method, including geometry optimization and vibrational analysis for the involved stationary points on the potential energy surface. The energies of the different conformations are calculated with CCSD(T)//MP2/6‐31G* method. From the potential energy profile, it can be predicted that the dominant reaction pathway of the cycloadditional reaction between singlet dimethylmethylene carbene and formaldehyde consists of two steps: (1) the two reactants(R1, R2) firstly form an energy‐enricheded intermediate (INT1a) through a barrier‐free exothermic reaction of ΔE = 11.3 kJ/mol. (2) Intermediate (INT1a) then isomerizes to a three‐membered product (P1) via a transition state (TS1a) with an energy barrier of 20.0 kJ/mol. The dominant reaction has an excellent selectivity and differs considerably from its competitive reactions in reaction rate. © 2009 Wiley Periodicals, Inc. Int J Quantum Chem, 2010     

Ab initio study of mechanism of forming germanic bis-heterocyclic compound between germylene carbene (H2GeC:) and acetone

The mechanism of the cycloaddition reaction of forming germanic bis-heterocyclic compound between singlet germylene carbene and acetone has been investigated with MP2/6-31G* method, including geometry optimization and vibrational analysis for the involved stationary points on the potential energy surface. The energies of the different conformations are calculated by CCSD (T)//MP2/6-31G* method. From the potential energy profile, it can be predicted that the dominant reaction pathway of the cycloadditional reaction of forming germanic bis-heterocyclic compound consists of three steps: (1) the two reactants firstly form an intermediate INT4 through a barrier-free exothermic reaction of 181.4 kJ/mol; (2) INT4 further reacts with acetone (R2) to form an intermediate (INT5), which is also a barrier-free exothermic reaction of 148.9 kJ/mol; (3) INT5 then isomerizes to a germanic bis-heterocyclic product P5 via a transition state TS5 with an energy barrier of 53.3 kJ/mol.     

Direct electrocatalytic reduction of hydrogen peroxide at a glassy carbon electrode modified with polypyrrole nanowires and platinum hollow nanospheres

A nonenzymatic sensor for hydrogen peroxide has been fabricated by dispersing platinum hollow nanospheres onto polypyrrole (PPy) nanowires to form a PPy-Pt hollow sphere nanocomposite on a glassy carbon electrode. The materials were characterized by transmission electron microscopy and scanning electron microscopy. The process and the sensor were characterized by electrochemical impedance spectroscopy, cyclic voltammetry, and chrono-amperometry and revealed that the electrode has a large electroactive surface area and small resistance to electron transfer. The linear range for the determination of hydrogen peroxide is from 3.5 µM to 9.9 mM, the detection limit is 1.2 µM (S/N?=?3), and the response time is 3 s. The electrode exhibited good stability and excellent repeatability.     

Phosphoric acid doped high temperature proton exchange membranes based on sulfonated polyetheretherketone incorporated with ionic liquids

A composite membrane was fabricated using a novel approach based on the ionic liquids 1-butyl-3-methylimidazolium chloride or 1-butyl-3-methylimidazolium hexafluorophosphate, sulfonated polyetheretherketone (SPEEK), and phosphoric acid. This proton conducting composite membrane shows promise for operation in high temperature proton exchange membrane fuel cells at working temperatures up to 160 °C without humidification. Proton conductivity at a level of 2.0 × 10^? 2 S/cm was achieved at 160 °C by the composite membrane with a molar ratio of 1:0.6:9 for SPEEK, 1-butyl-3-methylimidazolium (BMIM) cation and phosphoric acid, respectively. The sulfonation degree was 0.643 per polymer repeat unit with over 90% of the sulfate fixed anions forming a salt complex with BMIM cations. The tensile stress at break of the composite membrane was 15.5 MPa at room temperature, and it decreased from 4.1 to 1.9 MPa when the temperature increased from 110 to 160 °C, respectively.     

All-solid-state Nd:Gd<Subscript>0.18</Subscript>Y<Subscript>0.82</Subscript>VO<Subscript>4</Subscript>-LBO green laser at 532 nm

We report a continuous-wave (CW) coherent green radiation at 532 nm by intracavity frequency doubling generation of 1064 nm Nd:Gd_0.18Y_0.82VO₄ laser. With incident pump power of 18.2 W, output power of 1.08 W at 532 nm has been obtained using a 5 mm-long KTP crystal. The optical conversion efficiency was up to 5.9%. At the output power level of 1.08 W, the output stability is better than 5%. The beam quality M² values were equal to 1.26 and 1.12 in X and Y directions, respectively.     

Diode-pumped Nd:LGS intracavity-doubled green laser at 532 nm

It is reported that efficient continuous-wave (CW) green laser generation at 532 nm in a KTP crystal at type-II phase matching direction performed with a diode-pumped Nd:LGS laser. With incident pump power of 18.2 W, output power of 2.68 W at 532 nm has been obtained using a 5 mm-long KTP crystal. The optical conversion efficiency was up to 14.7%. At the output power level of 2.68 W, the output stability is better than 3.5%. The beam quality M ² values were equal to 1.33 and 1.19 in X and Y directions, respectively.     

Dual-wavelength laser operation at 1061 and 942 nm in Nd:GSAG

A dual-wavelength continuous-wave (CW) diode end-pumped gadolinium scandium aluminum garnet (Nd:GSAG) laser that generates simultaneous laser action at the wavelengths 1061 and 942 nm is demonstrated. A total output power of 589 mW (476 mW at 1061 nm and 113 mW at 942 nm) for the dual-wave-length was achieved at the incident pump power of 18.2 W. The M ² values for 942 and 1061 nm lights were found to be around 1.18 and 1.37, respectively.     

A study of the effect of laser beam geometries on laser bending of sheet metal by buckling mechanism

Laser beam forming has emerged as a new and very promising technique to form sheet metal by thermal residual stresses. The objective of this work is to investigate numerically the effect of rectangular beam geometries, with different transverse width to length aspect ratio, on laser bending process of thin metal sheets, which is dominated by buckling mechanism. In this paper, a comprehensive thermal and structural finite element (FE) analysis is conducted to investigate the effect that these laser beam geometries have on the process and on the final product characteristics. To achieve this, temperature distributions, deformations, plastic strains, stresses, and residual stresses produced by different beam geometries are compared. The results suggest that beam geometries play an important role in the resulting temperature distributions on the workpiece. Longer beam dimensions in the scanning direction (in relation to its lateral dimension) produce higher temperatures due to longer beam–material interaction time. This affects the bending direction and the magnitude of the bending angles. Higher temperatures produce more plastic strains and hence higher deformation. This shows that the temperature-dependent yield stress plays a more dominant role in the deformation of the plate than the spread of the beam in the transverse direction. Also, longer beams have a tendency for the scanning line to curve away from its original position to form a concave shape. This is caused by buckling which develops tensile plastic strains along both ends of the scanning path. The buckling effect produces the opposite curve profile; convex along the tranverse direction and concave along the scanning path.