Information Theory of Molecular Systems

Front Cover
Elsevier, Mar 31, 2006 - Science - 462 pages
As well as providing a unified outlook on physics, Information Theory (IT) has numerous applications in chemistry and biology owing to its ability to provide a measure of the entropy/information contained within probability distributions and criteria of their information "distance" (similarity) and independence. Information Theory of Molecular Systems applies standard IT to classical problems in the theory of electronic structure and chemical reactivity.

The book starts by introducing the basic concepts of modern electronic structure/reactivity theory based upon the Density Functional Theory (DFT), followed by an outline of the main ideas and techniques of IT, including several illustrative applications to molecular systems. Coverage includes information origins of the chemical bond, unbiased definition of molecular fragments, adequate entropic measures of their internal (intra-fragment) and external (inter-fragment) bond-orders and valence-numbers, descriptors of their chemical reactivity, and information criteria of their similarity and independence.

Information Theory of Molecular Systems is recommended to graduate students and researchers interested in fresh ideas in the theory of electronic structure and chemical reactivity.

·Provides powerful tools for tackling both classical and new problems in the theory of the molecular electronic structure and chemical reactivity·Introduces basic concepts of the modern electronic structure/reactivity theory based upon the Density Functional Theory (DFT)·Outlines main ideas and techniques of Information Theory

 

Contents

INTRODUCTION
1
body
28
ENTROPY INFORMATION AND COMMUNICATION CHANNELS
56
PROBING THE MOLECULAR ELECTRON DISTRIBUTIONS
91
ATOMSINMOLECULES FROM THE INFORMATION THEORY
118
OTHER PROPERTIES OF STOCKHOLDER SUBSYSTEMS
169
COMMUNICATION THEORY OF THE CHEMICAL BOND
201
ENTROPYINFORMATION INDICES OF MOLECULAR FRAGMENTS
244
REACTIVE SYSTEMS
293
ELEMENTS OF THE INFORMATIONDISTANCE THERMODYNAMICS
327
back matter
359
REFERENCES
421
INDEX
434
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Page 421 - Albright, TA, Burdett, JK, and Whangbo, M.-H. (1985). Orbital Interactions in Chemistry, John Wiley & Sons, New York.
Page 47 - Eq. (1.5.22) identifies the F-conjugate of the ground-state density p, ie, the local "intensity" defined by the functional derivative of F[p], as the negative relative external potential, -u, while the corresponding kernel of the second functional derivatives is given by the hardness kernel rj(r, r*) [Eq.
Page 34 - For example, the origin of chemical bonding, identity of AIM, factors determining the nature and relative importance of alternative reaction sites and pathways in large reactive and catalytic systems, stability of molecular charge distribution, similarity of molecules, electron localization...

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About the author (2006)

Roman F. Nalewajski is now Professor (Emeritus) of theoretical chemistry at Jagiellonian University in Cracow (Poland). His current research concerns mainly conceptual and methodological issues in quantum chemistry, and particularly density-functional theory (DFT) and information theory (IT) with applications to problems of the chemical bond, molecular electronic structure, and reactivity preferences. His recent interests focus on communication theory of the chemical bond, applying IT in chemical interpretations of molecular states and reactivities, and exploring the phase-equilibria in molecules or their fragments. He is the Author of about 250 scientific publications, two academic textbooks on quantum chemistry (in Polish) and five monographs (in English).

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