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Titlebook: Derivative Spectrophotometry and Electron Spin Resonance (ESR) Spectroscopy for Ecological and Biolo; Vladimir S. Saakov,Valery Z. Drapkin

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發(fā)表于 2025-3-21 19:23:55 | 只看該作者 |倒序?yàn)g覽 |閱讀模式
書目名稱Derivative Spectrophotometry and Electron Spin Resonance (ESR) Spectroscopy for Ecological and Biolo
編輯Vladimir S. Saakov,Valery Z. Drapkin,Mikhail N. Kn
視頻videohttp://file.papertrans.cn/269/268130/268130.mp4
概述Gives a modern approach to practical application of high order derivative spectro-photometry and ESR spectroscopy.Provides a clear overview of the basic methods.Practical applications of spectroscopic
圖書封面Titlebook: Derivative Spectrophotometry and Electron Spin Resonance (ESR) Spectroscopy for Ecological and Biolo;  Vladimir S. Saakov,Valery Z. Drapkin
描述This book provides a multidisciplinary overview to the application of high order derivative spectrophotometry and Electron Spin Resonance (ESR) spectroscopy in biology and ecology. The characteristics of the principle methods as well as the generation of reliable spectra are discussed in general terms allowing the reader to gain an idea of these methods’ potentials. Furthermore the authors give an extended overview to the spectroscopic and spectro-photometric analysis of specific biological materials. This volume is a well condensed description of an analytical method and a clear review to its application in biology and related fields and an essential tool for researchers who are new in the field of spectroscopic methods and their applications in the life sciences.
出版日期Book 2013
關(guān)鍵詞ESR spectroscopy; derivative spectrophotometry; higher order derivative spectrophotometry
版次1
doihttps://doi.org/10.1007/978-3-7091-1007-2
isbn_softcover978-3-7091-1709-5
isbn_ebook978-3-7091-1007-2
copyrightSpringer-Verlag Wien 2013
The information of publication is updating

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沙發(fā)
發(fā)表于 2025-3-21 21:36:57 | 只看該作者
978-3-7091-1709-5Springer-Verlag Wien 2013
板凳
發(fā)表于 2025-3-22 00:42:49 | 只看該作者
Introduction,ll, by the fact that they are relatively universal objects of research and allow one to obtain information on a biological system state at the atomic/molecular level after changes made by both natural and technogenic factors.
地板
發(fā)表于 2025-3-22 06:04:18 | 只看該作者
5#
發(fā)表于 2025-3-22 11:40:00 | 只看該作者
Conclusion,Thus, we come to the end of this book. And, if the reader had enough patience to reach this page, then he probably got information that is useful to him.
6#
發(fā)表于 2025-3-22 16:24:45 | 只看該作者
Jeffrey D. Markey,Jon Robitschekll, by the fact that they are relatively universal objects of research and allow one to obtain information on a biological system state at the atomic/molecular level after changes made by both natural and technogenic factors.
7#
發(fā)表于 2025-3-22 17:15:52 | 只看該作者
Jeffrey D. Markey,Jon Robitschekll, by the fact that they are relatively universal objects of research and allow one to obtain information on a biological system state at the atomic/molecular level after changes made by both natural and technogenic factors.
8#
發(fā)表于 2025-3-22 23:09:00 | 只看該作者
Analgesia and Conscious Sedationght flux intensity, ., and wavelength, λ are used in optical measurements. The frequency index . is also considered to characterize an absorbed light. Frequency is expressed in reciprocal seconds [c.] and presents itself as the ratio of a radiation velocity . to a wavelength λ [cm or nm]:.where . =3
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發(fā)表于 2025-3-23 02:21:37 | 只看該作者
Facial Plastic and Reconstructive Surgeryphysics, radiochemistry, and physical chemistry in physiological and biochemical experiments a scientist should find out for what fundamental research the analytical methods of related sciences are necessary, and what theoretical questions of modern physical-chemical biology cannot be answered witho
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發(fā)表于 2025-3-23 05:42:05 | 只看該作者
Sim Choroomi B.S.C. (Med)., M.B.B.S., FRACShophylls in the plant cell. This interest was caused by the fact that the earlier described light reaction of direct reduction without intermediate products of violaxanthin (5,6,5′,6′-diepoxy-5,5′,6,6′-tetrahydro-β-carotene-3,3′-diol) into lutein (3,3′-dihydroxy-α- carotene, β,ε-carotene-3,3′-diol)
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