Development and Application of Ultrafast Circular Dichroism Spectroscopy Techniques

Chirality hold broad applications in life sciences,quantum devices,and various other areas.Traditionally,molecular chirality can be characterized by using steady-state circular dichroism spectroscopy.However,the techniques that can characterize excited state chirality are progressively capturing the public interest as it can provide the dynamic information for chirality generation and transfer.In this review,we focus on the theoretical background and the developmental history of femtosecond time-resolved circular dichroism spectroscopy(TRCD)techniques around the world.Additionally,we provide examples to showcase the utility of these techniques in the analysis of the dynamical molecular chemical structures,the investigation of molecular chirality generation,and the detection of electron spin dynamics in semiconductor quantum dots.

Research Progress on Material Basis,Pharmacological Effect and Clinical Application of Danggui Shaoyao Powder

The research of modern pharmacology displays that main material basis of Danggui Shaoyao Powder exerting efficacy includes ligustilide,paeoniflorin,poria acid,ferulic acid,ligustrazine and so on,and its efficacy is mainly realized by regulating neural receptor-ligand interaction,cytokine release,and TNF-αinflammatory pathway.Systematic study of metabonomics,serum pharmacochemistry and network pharmacology of Danggui Shaoyao Powder sufficiently clarifies its potential pharmacodynamic mechanism,and it could provide scientific theoretical basis for its clinical application.In this paper,by systemically analyzing material basis of Danggui Shaoyao Powder,and exploring its complex pharmacological mechanism and clinical application in vivo,it could comprehensively understand the clinical value of Danggui Shaoyao Powder,so as to provide beneficial reference for further development of the material basis,quality control and classical prescription of Danggui Shaoyao Powder.

Direct Observation of Singletππ*and nπ*Equilibrium State in 2-Amino-1,3,5-triazine Solution

1,3,5-Triazine molecules represent a class of molecules that may have been prebiotic information carriers in a primordial soup in early Earth and their excited state dynamics has received attention in recent years.In our previous study,one component with lifetime longer than100 ps was discovered in 2-amino-1,3,5-trainzine(2-AT),but its nature has not been revealed.In this study,excited state dynamics of 2-AT is studied in different solvents by using femtosecond time-resolved transient absorption and fluorescence upconversion spectroscopy.Interestingly,an equilibrium state consisting of the brightππ^(*)and dark nπ^(*)states in 2-AT is directly observed in aqueous solution and its dynamics is solvent sensitive.The whole picture of the excited state deactivation mechanism of 2-AT is proposed based on our spectroscopy results.

Fluorescence dynamics of N-terminal Trp–Trp residues in polypeptide: intrinsic indicators for monitoring p H

pH plays a vital role in various cellular activities, and real-time observation of the intracellular p H through a p H indicator is very important for studying many physiological processes. In this paper, we studied the p H response of Trp–Trp dipeptide and its derivatives(NATrp_2Me, NBTrp_2 and Trp_2Me) by steady-state and time-resolved fluorescence spectroscopy. Both the fluorescence intensities and lifetimes of Trp–Trp dipeptide as well as Trp2 Me were functions of p H in the physiological range from 5.5 to 9.0. However, NATrp_2 Me and NBTrp_2 showed no difference. The exposed amino was found to be pivotal for its p H dependence. Moreover, an artificially synthesized tetrapeptide(Trp–Trp–Ala–Ser) confirmed the p H sensitivity of N-terminal Trp–Trp residues. The p H values could be quantitatively determined from the fluorescence intensities and lifetimes of the N-terminal Trp–Trp residue. Thus, the N-terminal Trp–Trp residues may be fused into the polypeptides/proteins to serve as an intrinsic p H indicator in fluorescence spectroscopy and imaging.