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排序方式: 共有143条查询结果,搜索用时 15 毫秒
1.
Stortelder A Buijs JB Bulthuis J van der Vies SM Gooijer C van der Zwan G 《Journal of photochemistry and photobiology. B, Biology》2005,78(1):53-60
The time-resolved fluorescence properties of the bacteriophage T4 capsid protein gp23 are investigated. The structural characteristics of this protein are largely unknown and can be probed by recording time-resolved and decay-associated fluorescence spectra and intensity decay curves using a 200 ps-gated intensified CCD-camera. Spectral and decay data are recorded simultaneously, which makes data acquisition fast compared to time-correlated single-photon counting. A red-shift of the emission maximum within the first nanosecond of decay is observed, which can be explained by the different decay-associated spectra of fluorescence lifetimes of the protein in combination with dipolar relaxation. In addition, iodide quenching experiments are performed, to study the degree of exposure of the various tryptophan residues. A model for the origin of the observed lifetimes of 0.032 +/- 0.003, 0.39 +/- 0.06, 2.1 +/- 0.1 and 6.8 +/- 0.8 ns is presented: the 32 ps lifetime can be assigned to the emission of a buried tryptophan residue, the 0.4 and 2.1 ns lifetimes to two partly buried residues, and the 6.8 ns lifetime to a single tryptophan outside the bulk of the folded gp23. 相似文献
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Stacey M. Frumm Zi Peng Fan Kenneth N. Ross Jeremy R. Duvall Supriya Gupta Lynn VerPlank Byung-Chul Suh Edward Holson Florence F. Wagner William B. Smith Ronald M. Paranal Christopher F. Bassil Jun Qi Giovanni Roti Andrew L. Kung James E. Bradner Nicola Tolliday Kimberly Stegmaier 《Chemistry & biology》2013,20(5):713-725
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Saskia Menzel Konstantinos D. Demadis Christoph Janiak 《Phosphorus, sulfur, and silicon and the related elements》2020,195(10):830-835
AbstractThe fully deprotonated anion of 1,3,5-benzene-triphosphonic acid 1,3,5-C6H3[PO32?]3 gives rise to deceptively simple 1H and 31P NMR spectra due to a corresponding [AX]3 spin system. The 13C{1H} NMR spectrum reveals two 13C isotopomers which are identified via AXX′2 systems. Results from analysis and iteration are described. 相似文献
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We present energy spectra of electrons formed in the reaction of He(23 S, 21 S) with NO2 which have significantly improved counting statistics and resolution compared to earlier work. Further, we show spectra of the fluorescence light emitted in these reactions. The data are recorded in the same molecular beam apparatus as the electron spectra. For the metastable singlet state He(21 S) the spectra have not been measured before. We find that in addition to ionization excitation transfer takes place into Rydberg states of NO2**. Subsequently, the highly excited NO2** molecules dissociate into NO and atomic O* Rydberg atoms. 相似文献
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Synthesis of Inorganic Structural Isomers By Diffusion‐Constrained Self‐Assembly of Designed Precursors: A Novel Type of Isomerism 下载免费PDF全文
Marco Esters Matti B. Alemayehu Zachary Jones Dr. N. T. Nguyen Dr. Michael D. Anderson Corinna Grosse Prof. Saskia F. Fischer Prof. David C. Johnson 《Angewandte Chemie (International ed. in English)》2015,54(4):1130-1134
The structure of precursors is used to control the formation of six possible structural isomers that contain four structural units of PbSe and four structural units of NbSe2: [(PbSe)1.14]4[NbSe2]4, [(PbSe)1.14]3[NbSe2]3[(PbSe)1.14]1[NbSe2]1, [(PbSe)1.14]3[NbSe2]2[(PbSe)1.14]1[NbSe2]2, [(PbSe)1.14]2[NbSe2]3[(PbSe)1.14]2[NbSe2]1, [(PbSe)1.14]2[NbSe2]2[(PbSe)1.14]1[NbSe2]1[(PbSe)1.14]1[NbSe2]1, [(PbSe)1.14]2[NbSe2]1[(PbSe)1.14]1[NbSe2]2[(PbSe)1.14]1[NbSe2]1. The electrical properties of these compounds vary with the nanoarchitecture. For each pair of constituents, over 20 000 new compounds, each with a specific nanoarchitecture, are possible with the number of structural units equal to 10 or less. This provides opportunities to systematically correlate structure with properties and hence optimize performance. 相似文献
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Speed S Vicente R Aravena D Ruiz E Roubeau O Teat SJ El Fallah MS 《Inorganic chemistry》2012,51(12):6842-6850
The syntheses, structural characterization, and magnetic behavior of two new hexanuclear copper(II) complexes derived from R-phosphonic acids and 1,3-bis(dimethylamino)-2-propanol (Hbdmap) with formulas [Cu(6)(μ-bdmap)(3)(μ(3)-Ph-PO(3))(2)(μ(3)-O···H···μ(3)-O)(ClO(4))(2)(H(2)O)]·5H(2)O (1) and [Cu(6)(μ-bdmap)(3)(μ(3)-t-Bu-PO(3))(2)(μ(3)-O···H···μ(3)-O)(μ(1,3)-dca)(dca)(H(2)O)]·6H(2)O (2) (Ph-H(2)PO(3) = phenylphosphonic acid, t-Bu-H(2)PO(3) = tert-butylphosphonic acid, dca = dicyanamide) are reported. Compounds 1 and 2 are hexanuclear 3.111 R-phosphonate(2-)/1,3-bis(dimethylamino)-2-propanolato(1-) cages including in the center the [μ(3)-O···H···μ(3)-O](3-) unit. The temperature dependence of the magnetic properties of 1 and 2 clearly indicates an overall strong antiferromagnetic coupling confirmed by DFT calculations. 相似文献
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