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91.
Parajuli Prakash Acharya Sanjit Shamshina Julia L. Abidi Noureddine 《Cellulose (London, England)》2021,28(12):7559-7577
Cellulose - In this study, alkali and alkaline earth metal chlorides with different cationic radii (LiCl, NaCl, and KCl, MgCl2, and CaCl2) were used to gain insight into the behavior of cellulose... 相似文献
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Michael Koch Karthikeyan Perumal Dr. Olivier Blacque Dr. Jai Anand Garg Dr. Ramanathan Saiganesh Dr. Senthamaraikannan Kabilan Prof. Dr. Kallupattu Kuppusamy Balasubramanian Dr. Koushik Venkatesan 《Angewandte Chemie (International ed. in English)》2014,53(25):6378-6382
Design of highly efficient phosphorescent emitters based on metal‐ and heavy atom‐free boron compounds has been demonstrated by taking advantage of the singlet fission process. The combination of a suitable molecular scaffold and appropriate electronic nature of the substituents has been utilized to tailor the phosphorescence emission properties in solution, neat solid, and in doped PMMA thin films. 相似文献
95.
Back Cover: Yoctoliter Thermometry for Single‐Molecule Investigations: A Generic Bead‐on‐a‐Tip Temperature‐Control Module (Angew. Chem. Int. Ed. 13/2014)
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96.
Mahamood K. Nadira Divya P. V. Vineethkumar V. Prakash V. 《Journal of Radioanalytical and Nuclear Chemistry》2020,324(3):949-961
Journal of Radioanalytical and Nuclear Chemistry - The activity concentration of natural radionucides such as 40K, 226Ra and 232Th and radon surface and mass exhalation rates of the soil were... 相似文献
97.
K. Kasi Amarnath Reddy Smriti Moi Ashwini Dolle Basavaprabhu Hosamani Kiran Krishnamurthy Sunita Prakash Srinivasarao Raghothama Konkallu Hanumae Gowd 《Helvetica chimica acta》2020,103(7):e2000062
Dimedone is the most widely used chemical probe for detection of cysteine sulfenic acid in peptides and proteins. The reaction of dimedone with cysteine sulfenic acid results in the formation of unique cysteine dimedone motif containing thioether bridge. Based on the structure of cysteine dimedone residue in polypeptide, a new building block of Fmoc-Cys(Dmd)-OH was developed for solid phase synthesis of peptide cysteine dimedone. Mass spectrometric sequencing of synthetic peptides have confirmed successful incorporation of cysteine dimedone in peptide chain using HBTU/HOBt as a coupling agent. The new method permits synthesis of peptides containing both cysteine thiol and cysteine dimedone in the same sequence which was difficult to achieve by conventional methods. The synthetic peptide of glutathione cysteine dimedone was used as a standard in probing the air-mediated oxidation of thiol to disulfide form of glutathione. The co-elution of standard peptide and reaction mixture of oxidation of glutathione in presence of dimedone using RP-HPLC have confirmed the formation of glutathione cysteine sulfenic as an intermediate in the air-mediated oxidation of glutathione. The synthetic peptides of cysteine dimedone may find application in the field of redox proteomics and generation of antibodies against modified cysteine residue. 相似文献
98.
Ram Singh Prakash Biswas Prateek K. Jha 《International journal of quantum chemistry》2020,120(14):e26239
Extensive density functional theory calculations are performed to analyze the structure and activity of Cu and Cu Zn/Cu ZnO clusters containing up to 10 Cu/Zn atoms. The minimum-energy structures of Cu Zn and Cu ZnO clusters are found by doping minimum-energy pure Cu clusters with Zn atom(s) and ZnO molecule(s), respectively, followed by energy minimization of the resultant clusters. Odd-even alteration in properties that determine cluster stability/activity is observed with cluster size, which may be attributed to the presence/absence of unpaired electrons. The difference in behavior between Zn/ZnO doping can be interpreted in terms of charge transfer between atoms. Charge transfers from Zn to Cu in the Cu Zn clusters and from Cu and Zn atoms to O atom in Cu-ZnO clusters, which implies that the Cu atom acts as an electron acceptor in the Cu Zn clusters but not in the Cu ZnO clusters. Finally, the adsorption energies of glycerol and hydrogen on Cu Zn/Cu ZnO clusters are computed in the context of the use of Cu Zn/Cu ZnO catalysts in glycerol hydrogenolysis. Glycerol adsorption is generally found to be more energetically favorable than hydrogen adsorption. Dual-site glycerol adsorption is also observed in some of the planar clusters. Fundamental insights obtained in this study can be useful in the design of Cu Zn/Cu ZnO catalysts. 相似文献
99.
Hideyuki Tatsuno Kasper S. Kjr Kristjan Kunnus Tobias C. B. Harlang Cornelia Timm Meiyuan Guo Pavel Chbera Lisa A. Fredin Robert W. Hartsock Marco E. Reinhard Sergey Koroidov Lin Li Amy A. Cordones Olga Gordivska Om Prakash Yizhu Liu Mads G. Laursen Elisa Biasin Frederik B. Hansen Peter Vester Morten Christensen Kristoffer Haldrup Zoltn Nmeth Dorottya Srosin Szemes va Bajnczi Gyrgy Vank Tim B. Van Driel Roberto Alonso‐Mori James M. Glownia Silke Nelson Marcin Sikorski Henrik T. Lemke Dimosthenis Sokaras Sophie E. Canton Asmus O. Dohn Klaus B. Mller Martin M. Nielsen Kelly J. Gaffney Kenneth Wrnmark Villy Sundstrm Petter Persson Jens Uhlig 《Angewandte Chemie (International ed. in English)》2020,59(1):364-372
Iron N‐heterocyclic carbene (NHC) complexes have received a great deal of attention recently because of their growing potential as light sensitizers or photocatalysts. We present a sub‐ps X‐ray spectroscopy study of an FeIINHC complex that identifies and quantifies the states involved in the deactivation cascade after light absorption. Excited molecules relax back to the ground state along two pathways: After population of a hot 3MLCT state, from the initially excited 1MLCT state, 30 % of the molecules undergo ultrafast (150 fs) relaxation to the 3MC state, in competition with vibrational relaxation and cooling to the relaxed 3MLCT state. The relaxed 3MLCT state then decays much more slowly (7.6 ps) to the 3MC state. The 3MC state is rapidly (2.2 ps) deactivated to the ground state. The 5MC state is not involved in the deactivation pathway. The ultrafast partial deactivation of the 3MLCT state constitutes a loss channel from the point of view of photochemical efficiency and highlights the necessity to screen transition‐metal complexes for similar ultrafast decays to optimize photochemical performance. 相似文献
100.