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Chemistry in action = making molecul...

Liu, Lai Chung.

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Chemistry in action = making molecular movies with ultrafast electron diffraction and data science /

紀錄類型:	書目-電子資源 : Monograph/item
正題名/作者:	Chemistry in action/ by Lai Chung Liu.
其他題名:	making molecular movies with ultrafast electron diffraction and data science /
作者:	Liu, Lai Chung.
出版者:	Cham :Springer International Publishing : : 2020.,
面頁冊數:	xx, 239 p. :ill., digital ;24 cm.
內容註:	Chapter1: Introduction -- Chapter2: Methods: Experimental Techniques and Data Science -- Chapter3: Ultrafast Structural Dynamics of (EDO-TTF)2X -- Chapter4: Photocyclization Dynamics of Diarylethene -- Chapter5: Photoinduced Spin Crossover in Iron(II) Systems -- Chapter6: Future Work -- Chapter7: Conclusion.
Contained By:	Springer Nature eBook
標題:	Chemistry, Physical and theoretical. -
電子資源:	https://doi.org/10.1007/978-3-030-54851-3
ISBN:	9783030548513

Chemistry in action = making molecular movies with ultrafast electron diffraction and data science /
Liu, Lai Chung.

Chemistry in actionmaking molecular movies with ultrafast electron diffraction and data science /[electronic resource] :by Lai Chung Liu. - Cham :Springer International Publishing :2020. - xx, 239 p. :ill., digital ;24 cm. - Springer theses,2190-5053. - Springer theses..

Chapter1: Introduction -- Chapter2: Methods: Experimental Techniques and Data Science -- Chapter3: Ultrafast Structural Dynamics of (EDO-TTF)2X -- Chapter4: Photocyclization Dynamics of Diarylethene -- Chapter5: Photoinduced Spin Crossover in Iron(II) Systems -- Chapter6: Future Work -- Chapter7: Conclusion.

The thesis provides the necessary experimental and analytical tools to unambiguously observe the atomically resolved chemical reactions. A great challenge of modern science has been to directly observe atomic motions during structural transitions, and while this was first achieved through a major advance in electron source brightness, the information content was still limited and new methods for image reconstruction using femtosecond electron diffraction methods were needed. One particular challenge lay in reconciling the innumerable possible nuclear configurations with the observation of chemical reaction mechanisms that reproducibly give the same kind of chemistry for large classes of molecules. The author shows that there is a simple solution that occurs during barrier crossing in which the highly anharmonic potential at that point in nuclear rearrangements couples high- and low-frequency vibrational modes to give highly localized nuclear motions, reducing hundreds of potential degrees of freedom to just a few key modes. Specific examples are given in this thesis, including two photoinduced phase transitions in an organic system, a ring closure reaction, and two direct observations of nuclear reorganization driven by spin transitions. The emerging field of structural dynamics promises to change the way we think about the physics of chemistry and this thesis provides tools to make it happen.

ISBN: 9783030548513

Standard No.: 10.1007/978-3-030-54851-3doiSubjects--Topical Terms:

518364
Chemistry, Physical and theoretical.

LC Class. No.: QD453.3 / .L585 2020

Dewey Class. No.: 541.2

Chemistry in action = making molecular movies with ultrafast electron diffraction and data science /
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520 $a The thesis provides the necessary experimental and analytical tools to unambiguously observe the atomically resolved chemical reactions. A great challenge of modern science has been to directly observe atomic motions during structural transitions, and while this was first achieved through a major advance in electron source brightness, the information content was still limited and new methods for image reconstruction using femtosecond electron diffraction methods were needed. One particular challenge lay in reconciling the innumerable possible nuclear configurations with the observation of chemical reaction mechanisms that reproducibly give the same kind of chemistry for large classes of molecules. The author shows that there is a simple solution that occurs during barrier crossing in which the highly anharmonic potential at that point in nuclear rearrangements couples high- and low-frequency vibrational modes to give highly localized nuclear motions, reducing hundreds of potential degrees of freedom to just a few key modes. Specific examples are given in this thesis, including two photoinduced phase transitions in an organic system, a ring closure reaction, and two direct observations of nuclear reorganization driven by spin transitions. The emerging field of structural dynamics promises to change the way we think about the physics of chemistry and this thesis provides tools to make it happen.
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