Vacuum ultraviolet 178.7 nm emission in sodium vapour under two-photon resonance excitation

We have observed a fixed wavelength emission at 178.7 nm in sodium vapour under 578.7 nm two-photon resonance excitation. The proposed non-linear wave mixing scheme is described by _{178.7 nm} = 2_L + _{465.7 nm}; where _178.7 is the 178.7 nm photon frequency, _L is the laser-photon frequency, and _465.7 is the 465.7 nm photon frequency. This 465.7 nm emission comes from another six-wave mixing process involving two hyper-electronic Raman scattering photons. The excitation spectrum of the 178.7 nm emission has a typical multiwave mixing pattern with a competing effect appearing at higher temperatures under two-photon resonance excitation. Numerical analysis indicates that this vacuum ultraviolet emission has a poor phase-match condition that will depress the emission intensity to a certain extent. This makes the observation more difficult compared with other reported four-wave mixing generated emissions. Fortunately, on the one hand, it is enhanced by quasi-auto-ionization resonance when the 3s–5s transition is coupled to the sodium continuum by a 330.2 nm photon. On the other hand, its wavelength sits so close to the sodium Cooper minimum that weak absorption will not suppress this vacuum ultraviolet emission further.     

pH滴定-主成分回归法同时测定酚类同系物

本文利用pH滴定－主成分回归法同时测定了苯酚、邻苯二酚、邻苯三酚的混合物，结果良好。通过交差验证法，本文还对采样区间和采样间隔作了详细讨论。     

Comparison between the symmetry-correlation examination and the perturbation method

A comparison between the construction of symmetry-correlation diagrams and the perturbation method for studying chemical reactions is carried out. The perturbation method consists of decomposing the system Hamiltonian H into a sum, H = H₀ + H′. Various symmetry correlation schemes appearing in the literature may be explained by the nonuniqueness of the decomposition scheme. All symmetry selection rules may be viewed as the varieties. By examining the symmetry-correlation diagrams, processes under investigation may be called “forbidden” or “allowed,” depending on the topological feature. Of particular importance is the topology associated with the “avoided crossing.” By making the comparison, we can establish the correspondence of the two methods and conclude that the perturbation order furnishes the origin of the “forbiddenness” of a process.     

Avoided crossing and intermediate states in certain photochemical reactions

An attempt to classify various types of avoided surface crossings originally discussed by Salem and co-workers is presented. From the present scheme, an order-of-forbiddenness criterion regarding reactivity is established from a consideration of electron and orbital counting. Since the new classification is qualitatively related to the energy gap created in the avoided crossing, the classification appears to be more systematic and informative. Energy transfer processes involved in electronically excited states may also be rationalized by such an application. Three major mechanistic types are distinguished: concerted two-electron process, concerted one-electron process, and stepwise one-electron process involving an ionic-pair intermediate.     

Crystal Structure of a Supramolecular Complex Formed between 1-bromo-2-iodo-tetrafluoroethane and N,N,N′,N′-tetramethyl-ethylenediamine

X-ray analysis has revealed that N,N,N′,N′-tetramethyl-ethylenediamine 1 form donor–acceptor complex 3 with 1-bromo-2-iodo-tetrafluoroethane 2, in which the N X (X = Br, I) distances are longer than the average covalent bond length between X and N, but are also definitively shorter than the sum of the corresponding van der Waals radii of X and N, thus that indicating weak interactions between the nitrogen and bromine or iodine atoms. In our experimental section, a valuable method for recrystallization and collect X-ray data from crystals that easily exhibit decay and can be cracked is reported.     

Synthesis and pharmacological analysis of high affinity melatonin receptor ligands

We report the synthesis and radioligand binding analysis of a series of naphthalenic melatonin receptor ligands, N-[2-(7-alkoxy-2-methoxy-1-naphthyl)ethyl]propionamide. This series of ligands exhibits subpicomolar binding affinity to both MT1 and MT2 melatonin receptors expressed in chinese hamster ovary (CHO) cells.