Photodiode-Based Chua＇s Circuit with Light Controllability

We present a photodiode-based Chua＇s chaotic circuit that is controllable by light. The proposed circuit consists of an inductor, two passive capacitors, a photodiode-based variable resistor, and a positive feedback trans- conductor with negative nonlinearity. The chaotic dynamics of the circuit were verified by using the simulation program with integrated circuit emphasis analysis using the 0.35 #m complementary metal-oxide-semiconductor process parameters. The gain results （such as the time waveform~ frequency analysis, three-dimensional attractor, bifurcation and Lyapunov exponents diagrams） confirm that the chaotic behavior of the circuit could be controlled by light intensity via the photodiode-based variable resistor.     

A QUANTITATIVE EVALUATION OF ELASTIC WAVE IN SOLID BY STROBOSCOPIC PHOTOELASTICITY

We have developed a method for visually measuring and evaluating stresses emitted from an ultrasonic probe into a model solid similar to the actual material, by using image-processing techniques and stroboscopic photoelasticity. The visualization of wave stress (sound pressure) distribution can be achieved by synthesizing two photoelastic pictures, in which the directions of the principal axes of linear polariscopes are different by 45 degrees. The sound pressure field generated by commercial ultrasonic probes was measured by using the proposed method.     

THE ROLE OF ISSUE LINKAGE IN MANAGING NONCOOPERATING BASINS: THE CASE OF THE MEKONG

The Mekong River (MR) is the major water source in Southeast Asia, sharedby six countries. There is a rush, by riparian states, to acquire sources of alternative energy and other benefits to meet growing demands for water and energy. China and Myanmar have refused to cooperate fully in the MR Forum, leading to increase risks within the region. Development of the water resources of the MR Basin is the subject of intense debate both within the Mekong region and internationally. This paper investigates the concept of issue linkage to resolve unidirectional externalities in the MR. Using linked games, the paper shows that the downstream nations can consider the use of linkage as a form of side payment in achieving a basin‐wide agreement. While this approach supports the Integrated Water Resource Management‐based Basin Development Strategy adopted by the Mekong River Commission in April 2011 for managing the region's sustainability development, facts on the ground suggest that traditional issues to be linked may not be sufficient. The paper addresses this observation and suggests a cadre of issues, including nontraditional ones, to be analyzed in a future work.     

Solving a Class of Linearly Constrained Indefinite Quadratic Problems by D.C. Algorithms

Linearly constrained indefinite quadratic problems play an important role in global optimization. In this paper we study d.c. theory and its local approachto such problems. The new algorithm, CDA, efficiently produces local optima and sometimes produces global optima. We also propose a decomposition branch andbound method for globally solving these problems. Finally many numericalsimulations are reported.     

Zagreb indices of graphs

The first Zagreb index M₁(G) is equal to the sum of squares of the degrees of the vertices, and the second Zagreb index M₂(G) is equal to the sum of the products of the degrees of pairs of adjacent vertices of the underlying molecular graph G. In this paper, we obtain lower and upper bounds on the first Zagreb index M₁(G) of G in terms of the number of vertices (n), number of edges (m), maximum vertex degree (Δ), and minimum vertex degree (δ). Using this result, we find lower and upper bounds on M₂(G). Also, we present lower and upper bounds on M₂(G) +M₂(G) in terms of n, m, Δ, and δ, where G denotes the complement of G. Moreover, we determine the bounds on first Zagreb coindex M₁(G) and second Zagreb coindex M₂(G). Finally, we give a relation between the first Zagreb index and the second Zagreb index of graph G.     

Molecular and electronic structure of zwitterionic diamino-meta-quinonoid molecules

Quantum chemical calculations using molecular orbital (HF, CASSCF) and density functional theory (B3LYP) methods, in conjunction with the 6–311 + + G(d,p) basis set, have been applied to investigate the molecular and electronic structure of two diamino-meta-quinonoid molecules 1a and 2a, each containing a six-membered ring coupled with two exocyclic C = O bonds situated in a meta position, along with two amino substituents (NH₂ and NH-CH₃). It is confirmed that these substituted meta-quinone systems exhibit a zwitterionic structure in which the positively charged N-C-C(H)-C-N subunit, containing the two amino-groups, forms two chemical bonds with the negatively charged O-C-C(H)-C-O subunit. The negative charge amounts to about half of an electron. The charge separation has been approached in terms of geometries, vibrational frequencies, and electronic distribution. The ionization energy for molecule 1a is about 7.8±0.3eV. The quinonoid systems are essentially non-aromatic characterized by the NICS(+1) values of around 1.2 ppm.     

Regioselective Bridging Calix[6]arenes: Synthesis and X-ray Structure of Trisbridged Calix[6]arene

The preparation and characterization of gold nanoparticles (～6 nm in diameter) modified with mono-6-thio-β-cyclodextrin (II) is described. The resulting monolayer-protected gold nanoparticles are water-soluble and more stable. The concentration of II plays a crucial role for the distribution of the modified nanoparticles. When the ratio of concentration of II to HAuCl₄,[II]/[HAuCl₄] ≥ 0.93, a stable gold nanoparticle with uniform distribution and diameter of 6.0 ± 0.9 nm will be obtained. The recognition of modified gold nanoparticles to organic guest molecule is researched. The modified gold nanoparticles can make the electrochemical reduction current of nitrobenzene decrease and can be self-assembled in three-dimensional to form spherical clusters with ligand of methylene green.     

Relativistic Electron Acceleration in a Wake Field Generated by the Intense Femtosecond Laser Interaction with a Mixture Jet of Deuterium Clusters and Molecules

High energy electron acceleration in a wake field generated in the intense ultrashort （30fs） laser pulse cluster gas jet interaction is experimentally demonstrated. Relativistic electrons with energy of 60 MeV were observed. These high energy electrons split into two beams due to the relativistic self-focusing of the laser.     

Theoretical Investigation on Mechanism,Thermochemistry, and Kinetics of the Gas-phase Reaction of 2-Propargyl Radical with Formaldehyde

Gas-phase mechanism and kinetics of the reactions of the 2-propargyl radical(H2CCCH), an important intermediate in combustion processes, with formaldehyde were investigated using ab initio molecular orbital theory at the coupled-cluster CCSD(T)//B3LYP/6-311++G(3df,2p) method in conjunction with transition state theory(TST), variational transition state theory(VTST) and Rice-Ramsperger-Kassel-Marcus(RRKM) calculations for rate constants. The potential energy surface(PES) constructed shows that the H2CCCH+HCHO reaction has six main entrances, including two H-abstraction and four additional channels, in which the former is energetically more favorable. The H-abstraction channels slide down to two quite weak pre-complexes COM-01(-9.3 kJ/mol) and COM-02(-kJ/mol) before going via energy barriers of 71.3(T0/P1) and 63.9 kJ/mol(T0/P2), respectively. Two post-complexes, COM-1(-17.8 kJ/mol) and COM-2(-23.4 kJ/mol) created just after coming out from T0/P1 and T0/P2, respectively, can easily be decomposed via barrier-less processes yielding H2CCCH2+CHO(P1,-12.4 kJ/mol) and HCCCH3+CHO(P2,-16.5 kJ/mol), respectively. The additional channels occur initially by formation of four intermediate states, H2CCCHCH2O(I1, 1.1 kJ/mol), HCCCH2CH2O(I3, 4.5 kJ/mol), H2CCCHOCH2(I4, 10.2 kJ/mol), and HCCCH2OCH2(I6, 19.1 kJ/mol) via energy barriers of 66.3, 59.2, 112.2, and 98.6 kJ/mol at T0/1, T0/3, TOM, and TO/6, respectively. Of which two channels producing 14 and 16 can be ignored due to coming over tlie high barriers TOM and TO/6, respectively. The rate constants and product branching ratios for the low-energy channels calculated show that the H2CCCH+HCHO reaction is almost pressure-independent. Altliough the H2CCCH+HCHO→Ⅰ1 and H2CCCH+HCHO→Ⅰ3 channels become dominant at low temperature, however, they are less competitive channels at high temperature.