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Books > Science & Mathematics > Chemistry
The book covers in particular state-of-the-art scientific research
about product quality control and related health and environmental
safety topics, including human, animal and plant safety assurance
issues. These conference proceedings provide contemporary
information on the general theoretical, metrological and practical
issues of the production and application of reference materials.
Reference materials play an integral role in physical, chemical and
related type of measurements, ensuring their uniformity,
comparability and the validity of quantitative analysis as well as,
as a result, the objectivity of decisions concerning the
elimination of technical barriers in commercial and economic,
scientific and technical and other spheres of cooperation. The book
is intended for researchers and practitioners in the field of
chemistry, metrologists, technical physics, as well as for
specialists in analytical laboratories, or working for companies
and organizations involved in the production, distribution and use
of reference materials.
The elucidation of reaction mechanisms generally requires the
carefully designed control of molecular symmetry to distinguish
between the many possible reaction pathways. Making and Breaking
Symmetry in Chemistry emphasises the crucial role played by
symmetry in modern synthetic chemistry. After discussion of a
number of famous classical experiments, the advances brought about
by the introduction of new techniques, in particular NMR
spectroscopy, are exemplified in numerous cases taken from the
recent literature. Experimental verification of many of the
predictions made in Woodward and Hoffmann's explication of the
Conservation of Orbital Symmetry are described. Applications that
involve the breaking of molecular symmetry to resolve these and
other mechanistic problems in organic, inorganic and organometallic
chemistry are presented in the first sections of the book, together
with many examples of the detection of hitherto hidden
rearrangement processes.Subsequently, under the aegis of making
molecular symmetry, examples of the preparation of highly
symmetrical molecules found in the organic, organometallic or
inorganic domains are discussed. These include Platonic
hydrocarbons or boranes, tetrahedranes, cubanes, prismanes,
dodecahedrane, fullerene fragments such as corannulene, sumanene or
semibuckminsterfullerene, and other systems of unusual geometries
or bonding characteristics (Moebius strips, molecular brakes and
gears, Chauvin's carbomers, Fitjer's rotanes, persubstituted rings,
metal-metal multiple bonds, etc.). The text also contains vignettes
of many of the scientists who made these major advances, as well as
short sections that briefly summarise key features of important
topics that underpin the more descriptive material. These include
some aspects of chirality, NMR spectroscopy, and the use of
isotopic substitution to break molecular symmetry. A brief appendix
on point group symmetry and nomenclature is also helpfully
provided.
'Clary's account makes for fascinating reading, not least because
of its clear style and copious citation of primary sources and
original scientific articles. The author provides a compelling
narrative of ... Schroedinger's departure in 1933 from a highly
eminent position at the University of Berlin to a precarious,
untenured position at Magdalen College ... with political and
scientific considerations deftly woven together.' [Read Full
Review]ScienceErwin Schroedinger was one of the greatest scientists
of all time but it is not widely known that he was a Fellow at
Magdalen College, Oxford in the 1930s. This book is an
authoritative account of Schroedinger's time in Oxford by Sir David
Clary, an expert on quantum chemistry and a former President of
Magdalen College, who describes Schroedinger's remarkable life and
scientific contributions in a language that can be understood by
all. Through access to many unpublished manuscripts, the author
reveals in unprecedented detail the events leading up to
Schroedinger's sudden departure from Berlin in 1933, his arrival in
Oxford and award of the Nobel Prize, his dramatic escape from the
Nazis in Austria to return to Oxford, and his urgent flight from
Belgium to Dublin at the start of the Second World War.The book
presents many acute observations from Schroedinger's wife Anny and
his daughter Ruth, who was born in Oxford and became an
acquaintance of the author in the last years of her life. It also
includes a remarkable letter sent to Schroedinger in Oxford from
Adolf Hitler, thanking him for his services to the state as a
professor in Berlin. Schroedinger's intense interactions with other
great scientists who were also refugees during this period,
including Albert Einstein and Max Born, are examined in the context
of the chaotic political atmosphere of the time. Fascinating
anecdotes of how this flamboyant Austrian scientist interacted with
the President and Fellows of a highly traditional Oxford College in
the 1930s are a novel feature of the book.A gripping and intimate
narrative of one of the most colourful scientists in history,
Schroedinger in Oxford explains how his revolutionary breakthrough
in quantum mechanics has become such a central feature in 21st
century science.
In this book importance of Asymmetric Synthesis are given with
examples. It has underlined concepts developed starting with basic
principles of stereochemistry. It is based on drug required, four
methodologies are given. The text is written in a simple and lucid
style. The topics have been dealt with systematically,
diagrammatically and in a lucid language. The book is based on
three important principles. First, concepts and terminology used in
asymmetric synthesis, second, the four types of asymmetric
synthesis and third, applications of asymmetric synthesis.
Students, teachers and researchers need to understand the
methodology of asymmetric synthesis, because of the crucial role
this plays in the organic synthesis, especially in synthesis of
drugs. An understanding of different methods of asymmetric
synthesis is essential for the planning of drug synthesis using the
knowledge of QSAR.
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