Changlin Liu

Single crystal Si subsurface damage and phase transformation caused by laser-assisted nanometric cutting were investigated in this paper through the ultraprecision cutting experiments and molecular dynamics simulation. Post-cutting examination of a crystal's subsurface revealed a distorted SiI layer and an amorphous Si with embedded nanocrystalline Si-III and Si-XII. As a result of insufficient contact pressure during laser-assisted cutting, the amorphous Si was directly generated from the SiI through the collapse of the crystal lattice rather than from the intermediate high-pressure phase Si-II. The newly-formed amorphous Si crystallized partially during the laser-assisted cutting and transformed into metastable Si-III and Si-XII phases caused by the laser annealing effect. In comparison to machining without laser assistance, it was found that dislocation activity was increased by a factor of ~8 × 1014 when laser assistance was applied. This gave rise to enhancement of plastic deformability of the material, with the critical ductile-brittle transition depth of cut increasing from 150 nm to 395 nm and the thickness and extent of stress in the distorted SiI subsurface layer being reduced.

The binuclear structure of Fe(2)(DTPB)(mu-O)(mu-Ac)Cl(BF(4))(2) (DTPB = 1,1,4,7,7-penta (2'-benzimidazol-2-ylmethyl)-triazaheptane, Ac = acetate) was characterized by UV-visible absorption and infrared spectra and NMR and ESR. The binding interaction of DNA with the diiron complex was examined spectroscopically. Supercoiled and linear DNA hydrolytic cleavage by the diiron complex is supported by the evidence from anaerobic reactions, free radical quenching, high performance liquid chromatography experiments, and enzymatic manipulation such as T4 ligase ligation, 5'-(32)P end-labeling, and footprinting analysis. The estimation of rate for the supercoiled DNA double strand cleavage shows one of the largest known rate enhancement factors, approximately 10(10) against DNA. Moreover, the DNA hydrolysis chemistry needs no coreactant such as hydrogen peroxide. The poor sequence-specific DNA cleavage indicated by the restriction analysis of the pBR322 DNA linearized by the diiron complex might be due to the diiron complex bound to DNA by a coordination of its two ferric ions to the DNA phosphate oxygens, as suggested by spectral characterizations. The hydrolysis chemistry for a variety of binuclear metal complexes including Fe(2)(DTPB)(mu-O)(mu-Ac)Cl(BF(4))(2) is compared. It is established that the dominant factors for the DNA hydrolysis activities of the binuclear metal complexes are the mu-oxo bridge, labile and anionic ligands, and open coordination site(s). Concerning the hydrolytic mechanisms, the diiron complex Fe(2)(DTPB)(mu-O)(mu-Ac)Cl(BF(4))(2) might share many points in common with the native purple acid phosphatases.