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Book Review Dynamische Biochemie Teil II. (Dynamic Biochemistry Part II). By E

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energy follows, which treats the relationships between the
change in molecular geometry and the energy content. The
chapter closes with a critical discussion of conventional
molecular models.
Chapter 2, Stereoisomerism, opens with the sentence that is
fundamental to further understanding of the book: “Isomers
or structural isomers are defined as chemical species which
have the same molecular formula but differ in structure and
are separated by energy barriers”. Constitutional isomers and
stereoisomers are next distinguished (“Stereoisomerism arises
because molecules which have the same constitution may
still differ in the spatial arrangements of their atoms”) and
this is followed by the important definition: “Stereoisomers
which are related as object and nonsuperimposable mirror
image are called enantiomers or antipodes, whereas those
which are not so related are called diastereomers”. If this
widely based definition is accepted, the cis-trans olefins
designated as geometrical isomers in the past must now be
regarded as diastereomers. The chapter goes on to discuss
optical activity, including optical rotatory dispersion and
circular dichroism. A section that deserves special mention
is that describing rotational isomerism of single bonds
(conformational isomerism) in which two very useful terms
are coined. The terms enantiomeric and diastereomeric are
replaced in those cases where they refer to the stereochemistry
of the surroundings of an atom or group by enantiotopic and
diastereotopic. After a useful introduction to the stereochemistry of macromolecules, the chapter concludes with a
discussion of topoIogica1 isomerism (e.g. catenanes).
In Chapter 3 the main emphasis is placed on the development
and interpretation of the fundamentals of kinetic resolution
of racemates and asymmetric synthesis, and o n the determination of absolute configurations by both chemical and
physical methods.
A set of exercises is given at the end of each chapter, answers
following at the end of the book.
In its few pages the book provides an outline of modern
stereochemistry, and as a result the high information density
does not make for easy reading. True understanding and
appreciation of the material is possible only if the reader
works his way through the exercises, which are described by
the author as a n integral part of the book, since they are
designed to advance the student, through the inclusion of new
subject matter, beyond the descriptive material.
The broad definitions of stereoisomerism and diastereomerism are very useful for the advanced reader, but are
difficult to understand for the beginner because the subordinate terms geometrical isomerism, conformational isomerism, and “conventional” diastereomerism are used without sufficient discrimination.
Viewed as a whole, Mislow’s “Introduction” is too difficult
for the true beginner. For students preparing for their first
degree, however, the book is not only a valuable supplement
but a good textbook which offers fundamentals and results
of stereochemical research in concentrated and modern form.
In this sense the book can be recommended to all advanced
students and postgraduates. H . J. Bestmann
[NB 689 IE]
Kristallchemie (Crystal chemistry). By J. Zemann, Sammlung
Goschen, Vol. 1200/1220a, Walter de Gruyter & Co., Berlin 1966, 144 pp., 90 figures, paper covers, D M 5.80.
To fit a rapidly growing field of research such as crystal
chemistry into the framework of the Sammlung Goschen
necessitates the practice of the art of omission. The author
has deleted material in those realms in which even long
monographs and collective works prove unsatisfactory,
owing to the obvious impossibility of comprehensive treatment, e.g. in the compiling of special structural data. This
small book is intended mainly for chemists, for whom it
represents a well conceived introduction by virtue of its
lucid general chapters o n structural units and their bonding,
and the fundamental treatment and description of chemical
structures in the crystalline state. A desirable feature in future
editions would be the provision of space for discussing
additional material, e.g. the structure of molecules and
complexes or possibly crystallographic and chemical comparisons of transition metal compounds, for the benefit of
chemists taking an increasing interest in these problems.
H. G. v. Schnering
[NB 693 IEj
Die Anwendung der paramagnetischen Elektronenresonanz in
der Chemie (The Use of Paramagnetic Electron Resonance
in Chemistry). By L. A . Bournenfeld, V. V. Vojevodski and
A . G. Sernjonow. Translated from the Russian by K. Heuer
and Hannelore Heuer. Akademische Verlagsgesellschaft.
FrankfurtiMain 1966, 308 pages, 120figures, and 20 tables,
D M 55.-.
This book is addressed tothe readerwho wishes to use electron
resonance to solve his chemical problems. The monograph,
completed in 1961-1962 (with a few more recent additions
by the translators) consists of a predominantly theoretical
part (experimental technique, theory, evaluation of
results) and of a part dealing with the application of the
A relatively large amount of space is devoted to a description
of the design principles of the spectrometer. The chemist will
generally skip this chapter because a commercial instrument
is normally available. The theory of spectra (fine structure,
g-factor and its anisotropy) in crystals is discussed in detail.
whereas the anisotropic hyperfine structure and also the
isotropic hyperfine structure are dealt with rather briefly.
The treatment of the evaluation of the spectra is biased
toward the study of crystalline samples.
Few publications, and these nlostly the authors’ own, are
discussed to illustrate applications (chemical reactions.
delocalization phenomena, radiolysis of solids, kinetics, etc.).
This method prevents the inquiring chemist from becoming
confused by a mass of individual results and directs him to
fundamentals, but it does mean that he can seek solutions to
his own particular problems only in the literature, especially
in view of the year of publication of the original edition. The
reproduction of the spectra leaves something to be desired,
and the collection of the literature references at the end of
the book makes reading more difficult. In view of the quantity of theoretical and experimental work published in the
field during recent years the book only partially satisfies the
needs of research workers in this field. For the chemist who
wishes merely to familiarize himself with the method and its
possibilities, the book will prove to be a useful acquisition.
K. Scheffrer
[NB 692 IE]
Dynamische Biochemie, Teil 11. (Dynamic Biochemistry,
Part 11). By E. Hofmann. Wissenschaftliche Taschenbiicher.
Vol. 37. Akademie-Verlag. Berlin 1966. 1st Edit. 270
pages, 38 figures, 9 tables, paper covers, DM 12.50.
Among the pocket books published in recent years those of
the Akademie-Verlag, Berlin, are distinguished by thorough,
didactic editing and scientific accuracy. The volume “Dynamic Biochemistry, Part 11” describes the fundamentals of
protein and nucleic acid metabolism and the modern discoveries about cell make-up, regulation mechanisms, and
molecular biology in a concise, pregnant, and scientifically
impeccable manner. This well written book contains a n
amazing wealth of detail and interesting biochemical comparison material for such a small volume. Complicated
relationships are illustrated by means of clear, if necessarily
somewhat abridged diagrams. Even where the scope permits
only indications, they are never given merely as keywords.
Objections to modern interpretations are also discussed,
though it has of course not been possible to take into account
the results of the last two years, which have destroyed many
Angew. Chem. internal. Edit. Vol. 7 (1968) I No. 5
hypotheses. The one real feature whose absence will be felt
is a reference to the chemo-osmotic theory of oxidative
phosphorylations. Actual mistakes are neither frequent nor
significant. Particular mention is due t o the exceptionally
neat and faultless presentation, combined with the very
acceptable price. Every student interested in this (alas all too
often neglected) subject will be able to afford the sound
information contained in this excellent volume.
L. Juenicke
[NB 720 IE]
Mass Spectrometric Analysis of Solids. Edited by J . Ahenrn.
Elsevier Publishing Comuany, Amsterdam-London-New
York 1966. 1st Edit., viii, 175 pp., 46 figures, 13 tables,
Dfl. 30.-.
As a result of its high sensitivity, the simplicity of handling
samples, and the relative ease of interpreting spectra, mass
spectrometric analysis of solids is finding ever-increasing
fields of application. The present book, which comprises five
chapters written by experts, provides a review of the present
state of this field.
Chapter 1, by A . J . Ahearn, gives a general introduction t o
the subject. In Chapter 2, R . E. Honig treats the methods of
ion production used in analysis of solids. Methods of
evaluation and analytical errors are also dealt with insofar
as they are affected by the type of ion source. The use of
photographic plates in quantitative mass spectroscopic
analysis is decribed by E. B. Owens in Chapter 3, in which the
blackening process, properties of photoemulsions for ion
detection, density measurements, and methods for quantitative
evaluation of spectra receive a critical treatment. Chapter 4,
by J. W. Guthrie, deals with special analytical processes and
mentions investigations of liquids, organic substances, metals
of low melting point, as well as insulators and powders of
varying conductivity. Further, the application of standards
and measurements on very small samples are treated thoroughly. In thelast Chapter, W. M . Hickam and G . G. Sweeney
describe the application of the mass spectrograph as a
microprobe. In such work the surface of the sample is
examined by means of a tungsten tip, which serves as a
spark electrode. There is also a short section dealing with the
use of negative ions for analysis - a subject that is all too
often neglected.
The text is written clearly and concisely, and apart from
providing a general introduction it contains a wealth of data,
in the form of tables and diagrams, that will also be of value
to the expert. The bibliography at the end of each section is
also useful. The book can be recommended to all who are
concerned with analysis of solids, and particularly with trace
analysis, as well as to all libraries frequented by chemists
H. Hintenberger
[NB 696 IE]
and physicists.
Spectrometric Identification of Organic Compounds. By R . M.
Silverstein and G . C. Bassler, John Wiley and Sons, New
York-London-Sydney 1967, 2nd Edit., IX, 256 pages,
numerous illustrations, 75 s.
The publication of the 2nd edition of Silverstein-Bassler in
1967 follows four years after that of the 1st [I]. The aim and
presentation remain unaltered, but the text has been completely rewritten, the exercises revised and supplemented, and
numerous new figures, tables, and literature references inserted. Thus, practically all the shortcomings of the 1st
edition have been eliminated. It is only difficult to understand why the UV bands are still denoted by the out-ofdate system of Burawuy and why in the compilation of the
notations for the aromatic bands it is precisely those of CIar
and Plutt that are missing.
In view of the increasing importance attached to physical
methods in organic chemistry today, the trouble taken by the
authors in preparing the 2nd edition is extremely welcome.
Chapter 2 (Mass Spectroscopy) has been considerably exAngew. Chem. internut. Edit. VoI. 7 (1968) / No. 5
panded. All mass spectra are now shown graphically (instead
of in tabular form as previously), so that typical spectra are
much easier to recognize. Chapter 3 (IR Spectroscopy) clarifies
the discussion of characteristic group frequencies of individual
classes of compounds by reproducing more than 40 typical
spectra. Chapter 4 (NMR spectroscopy) contains new sections dealing with protons on heteroatoms, coupling of
protons with other nuclei, more complex spin-spin coupling,
chemically but not magnetically equivalent protons, effects
of an asymmetric center, virtual coupling, vicinal and geminal
coupling in rigid systems, long-range coupling, and spin-spin
In all chapters the data has been expanded and supplemented
t o such an extent that this excellent guide t o identification of
spectra will serve not merely as a text-book and exercise book
but also as a quick reference source for the organic chemist
in his laboratory. The book can be recommended without
reservation t o all who wish to learn about the application
of spectroscopic methods to structural problems in organic
chemistry, and t o those who use spectroscopic methods in
their research.
[N B 71 3 IE]
M. Klessinger
Organic Chemistry of Synthetic High Polymers. By R . W .
Lenz. Interscience Publishers, a Division of John Wiley &
Sons, New York-London-Sydney, 1967. 1st Edit., xvi,
837 pages, 120 s.
This book attempts for the first time t o present the entire
field, including up-to-date results, in very concise and clear
form. I n principle the attempt has succeeded. Having regard
to the vast amount of material covering such a wide range of
topics, it would have succeeded even better if more than three
of the chapters had been written by specialists. Some of the
chapters are very short and assume considerable knowledge.
To compensate, the most important literature references have
been included - though only a few Russian ones - enabling
the original works t o be studied.
A number of detailed objections may be raised, of which the
most important are the following: The gain recorded by the
new systematic classification of polyreactions (1.1 -1.3) over
older concepts is outweighed by the future confusion that will
arise, particularly for the non-specialist. The chapter dealing
with inorganic polymers (6.6) leads to a wrong emphasis by
omitting the most important classes. The degradation of a
cationic chain end with an anion (9-15, p. 245) is much more
like the degradation of a n anionic chain end with an electrophilic group than a radical recombination (9-13, p. 245).
A p-elimination (9-16, p. 245) does not represent a disproportionation. By contrast to anionic end groups, the
degradation reaction on free radical end groups is governed
by the probability of the collision of two chain ends, i.e.
purely thermodynamically; the comparison between “living
polymers” and relatively stable radicals (cf. p. 247) is therefore not justified.
A great advantage of the book is the strict classification of
the material and the generally concise and clear style. The
references t o model reactions involving species of low molecular weight that are given for many polyreactions are
extremely useful and the frequent numerical examples given
with the formulas contribute much t o the clarity of the book.
This welcome new publication undoubtedly enriches the
literature in this field and will find a wide readership.
G. Greber
[NB 711 IE]
Kinetics of Inorganic Reactions. By A. G . Sykes, Pergamon
Press. Oxford 1966, 1st Edit., viii. 310 pages, 35 figures,
42 tables, paper covers, 30 s.
The fields of chemistry which have recently emerged out of
the shadows into the limelight of general interest undoubtedly include that of inorganic reaction mechanisms. The
retail book trade provides as good a confirmation as any of
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