利用超快光谱与可见/红外双激发荧光对长寿命振动热基态的直接观察

在超快红外光谱测量中观察到的纳秒级弛豫诱导漂白信号被广泛认为是由于红外激发热化产生的局部热效应。本文结合超快红外泵浦/探测、二维红外光谱、可见泵浦/红外探测和超快可见/红外双共振荧光实验,发现甲醇溶液中荧光素二价阴离子的振动热基态寿命出人意料的长,能达到纳秒级.结果表明,在非线性红外实验中观察到的长寿命漂白信号在最初的几纳秒内一定存在这些热基态的重要贡献.类似的机制很可能也适用于其他分子系统,热基态的存在时间能比以往的预期长得多,有可能被应用于调控化学反应.

Intermolecular Vibrational Energy Transfers in Melts and Solutions

Resonant and nonresonant intermolecular vibrational energy transfers in Gdm- SCN/KSCN=1/1, GdmSCN/KS^13CN=1/1 and GdmSCN/KS^13C^15N=1/1 mixed crystals in melts and in aqueous solutions are studied with the two dimensional infrared spectroscopy. The energy transfers in the samples are slower with a larger energy donor/acceptor gap, independent of the Raman spectra. The energy gap dependences of the nonresonant energy transfers cannot be described by the phonon compensation mechanism. Instead, the experi- mental energy gap dependences can be quantitatively described by the dephasing mechanism. Temperature dependences of resonant and nonresonant energy transfer rates in the melts are also consistent with the prediction of the dephasing mechanism. The series of results suggest that the dephasing mechanism can be dominant not only in solutions, but also in melts （pure liquids without solvents）, only if the molecular motions （translations and rotations） are much faster than the nonresonant energy transfer processes.

Experimental Consideration of Two-Dimensional Fourier Transform Spectroscopy

Two-dimensional Fourier transform(2D FT) spectroscopy is an important technology that developed in recent decades and has many advantages over other ultrafast spectroscopy methods. Although 2D FT spectroscopy provides great opportunities for studying various complex systems, the experimental implementation and theoretical description of 2D FT spectroscopy measurement still face many challenges, which limits their wide application.Recently, the 2D FT spectroscopy reaches maturity due to many new developments which greatly reduces the technical barrier in the experimental implementation of the 2D FT spectrometer. There have been several different approaches developed for the optical design of the 2D FT spectrometer, each with its own advantages and limitations. Thus, a procedure to help an experimentalist to build a 2D FT spectroscopy experimental apparatus is needed.This tutorial review is intending to provide an accessible introduction for a beginner to build a 2D FT spectrometer.

Limits in Enhancement Factor in Near-Brewster Angle Reflection Pump-Probe Two-Dimensional Infrared Spectroscopy

In this work,we simulated 2D infrared spectroscopy(IR)spectroscopy in both transmission geometry and Brewster-angle reflection geometry.Light dispersion and the leakage of s-polarized light are considered in simulating the enhancement factor of the reflection mode.Our simulation shows that the dispersion in reflection will only alter the 2D IR lineshape slightly and can be corrected.Leaking spolarized light due to imperfectness of IR polarizers in the reflection geometry may limit the enhancement factor,but such limit is above what a typical experiment can reach.In the current experiment,the enhancement factor is mainly limited by the precision of incident angle,for which ordinary rotation stages are probably not adequate enough.Moreover,traditional energy ratio of pump and probe pulses,which is 9:1,may not be ideal and could be changed to 2:1 in the reflection geometry.Considering all the above factors,the enhancement on the order of 1000 is possible in the current experiment.Nevertheless,near-Brewster angle reflection will enhance both the signal and the noise caused by the signal itself,therefore this method only works if the noise is unrelated to the signal,particularly if the noise is caused by the fluctuation in the probe.It cannot improve the signal to noise ratio when the dominate noise is from the signal itself.The theoretical results here agree reasonably well with published experiment results and pave way for realizing even higher enhancement at nearer-Brewster angle.

Fabrication of PdSe2/GaAs Heterojunction for Sensitive Near-Infrared Photovoltaic Detector and Image Sensor Application

In this study,we have developed a high-sensitivity,near-infrared photodetector based on PdSe2/GaAs heterojunction,which was made by transferring a multilayered PdSe2 film onto a planar GaAs.The as-fabricated PdSe2/GaAs heterojunction device exhibited obvious photovoltaic behavior to 808 nm illumination,indicating that the near-infrared photodetector can be used as a self-driven device without external power supply.Further device analysis showed that the hybrid heterojunction exhibited a high on/off ratio of 1.16×10^5 measured at 808 nm under zero bias voltage.The responsivity and specific detectivity of photodetector were estimated to be 171.34 mA/W and 2.36×10^11 Jones,respectively.Moreover,the device showed excellent stability and reliable repeatability.After 2 months,the photoelectric characteristics of the near-infrared photodetector hardly degrade in air,attributable to the good stability of the PdSe2.Finally,the PdSe2/GaAs-based heterojunction device can also function as a near-infrared light sensor.

Two-Dimensional Infrared Spectroscopy of the Photoproduct of π-Cyclopentadienyliron Dicarbonyl Dimer

Equilibrium photoproduct of 7r-cyclopentadienyliron dicarbonyl dimer [CpFe（CO）2]2 in non- polar solvent carbon tetrachloride （CC14） is investigated using time-resolved 2D IR spec- troscopy. One of the several possible visible-light-driven photoreaction pathways is confirmed and the product is found to contain a di-carbonyl group that exhibits quantum beating be- tween two equivalent transitions in time-resolved 2D IR spectra, which turns out to be the anti-symmetric and symmetric stretching of the terminal carbonyl stretching modes of CpFe（CO）2C1. This is the main product and its reaction pathway involves radical formation, followed by chloride addition. Quantum-chemistry computations support these experimental results. Our results indicate that 2D IR method can be used to identify in situ structures and dynamics of chemical species involved in condensed-phase chemical reactions.

A new ketosteroid from red alga Acanthophora spicifera

A new ketosteroid, along with six known steroids, was isolated from the ethanolic extracts of red alga Acanthophora spicifera （Vahl.） Boergesen. The structures, identified using chemical and spectroscopic methods including 2D NMR, were： （1） 22-hydroxy-5α-eholest-3,6-dione, （2） 6-hydroxycholest-4-ene-3-one, （3） cholest-4-ene-3,6-dione, （4） cholest-5-ene-3β-ol, （5） 5u-cholestane-3,6-dione, （6） β-Sitosterol and （7） Saringosterol. The MTT method was used to test the cytotoxicity of the compounds against the human cancer cell lines, HCT-8, Bel-7402, BGC-823, A549 and HELA. Compounds 1, 2, 3 and 5 showed moderate cytotoxic activity against human cancer cell lines.

First Oxidation Product of Vitamin C, the Dehydro-L-Ascorbic Acid Dimer： A Study Based on FTIR-Raman and DFT Calculations

We studied the first oxidation product of vitamin C, the dehydro-L-ascorbic acid dimer and characterized it by infrared and Raman spectroscopies in the solid phase. The Density functional theory was used to study its structure and vibrational properties. These calculations gave us a precise knowledge of the normal modes of vibration taking into account that the molecule comprises a system of five fused rings; non planar γ-lactone and furonose rings are attached to a central dioxan ring in the twisted boat conformation. The calculated harmonic vibrational frequencies are consistent with the experimental vibrational spectra. An assignment of the observed spectral features is proposed. The shift of the band located in the infrared spectrum of the ascorbic acid from 3409 cm^-1 to 3299 cml and the remarkable increase in the band intensity at 1784 cm^-1 evidences the acid decomposition into its first product, the dehydro-L-ascorbic acid. The theoretical vibrational calculations allowed us to obtain a set of scaled force constants. The nature of the different -γ-lactone, furanose and dioxan rings and their topological properties were investigated by means of natural bond orbital and Bader＇s atoms in the molecule theory, respectively.

Selection of characteristic spectral bands for the analysis by the NIR correlation coefficient method

We analyzed the infrared 0R）-near infrared （NIR） 2D correlation spectra of drugs perturbed by temperature. By identification of functional groups by IR spectrum and by the correlation analysis of IR-NIR spectrum, we identified the characteristic spectral bands that were closely related to the structure of a drug substance of interest. These characteristic spectral bands were relatively less interfered by other ingredients for analysis by the NIR correlation coefficient method. With these characteristic spectral bands, the accuracy of screening illegally added Sildenafil citrate, Tadalafil and Metforrnin hydrochloride in Chinese patent drugs and healthcare products reached about 90%, which met the requirements of rapid screening.

Anharmonic vibrations of nucleobases: Structural basis of one-and two-dimensional infrared spectra for canonical and mismatched base pairs

Canonical Watson-Crick base pairs and four representative mismatched base pairs have been studied by quantum chemical computations. Detailed anharmonic vibrational analysis was carried out to reveal some vibrational signatures characteristic of structural aspects of the base monomers and dimers, which were well manifested in simulated 1D IR and 2D IR spectra. The degree of delocalization of the selected normal modes, represented by the potential energy distribution, was found to vary sig-nificantly from isolated bases to H-bonded dimers, and was accompanied by changes in anharmonicities of these modes. Examples are given for the generally accepted carbonyl stretching mode of base pairs appearing in the 6-m wavelength region of IR spectra.