Introductory References

Holloway, J. H. (1968). Noble-Gas Chemistry. Methuen, London. A thorough discussion of some of the early work on noble gas chemistry. A good introductory reference. 

Membranes play essential roies in the functions of both prokaryotic and eukaryotic cells. There is no unicellular or multicellular form of life that does not depend on one or more functional membranes. A number of viruses, the enveloped viruses, also have membranes. Cellular membranes are either known or suspected to be involved in numerous cellular functions, including the maintenance of permeability barriers, transmembrane potentials, active as well as specific passive transport across the membranes, hornione-receptor and transmitter-receptor responses, mitogenesis, and cell-cell recognition. The amount of descriptive material that might be included under the title of biological membranes is encyclopedic. The amount of material that relates or seeks to relate structure and function is less, but still large. For introductory references see Refs. 53, 38, 12, 47, 34, 13. Any survey of this field in the space and time available here is clearly out of the question. For the purposes of the present paper we have selected a rather narrow, specific topic, namely, the lateral diffusion of molecules in the plane of biological mem-branes.38,12,43,34 We consider this topic from the points of view of physical chemistry and immunochemistry. 

Specific references will be given at the end of each chapter. Here we list a series of general or introductory references. 

There are a number of references by Dr. Edward Calabrese introducing and arguing for the validity of the hormesis hypothesis. These include the BELLE Newsletter (Biological Effects of Low Level Exposure) published by Dr. Calabrese from the University of Massachusetts. Two good introductory references are these ... 

The chemistry of certain alkylphenols and that of hindered phenols has been discussed in chapter 6 where tabulated material has included introductory reference to compounds considered at length in the present chapter. Alkylphenols possessing longer alkyl chains which are sometimes mono- but usually multi-branched have achieved special industrial interest notably those with Cg and Cg alkyl groups in the 4-position such as 4-t-nonyl- and 4-t-octylphenol. In addition, 4-t-butylphenol has also attained a considerable level of commercial chemical interest and in recognition of the unique position of these types of compound their chemistry is now detailed. 

T. Boublik, I. Nezbeda, and K. Hlavaty, Statistical Thermodynamics of Simple Liquids and Their Mixtures, Elsevier, New York, 1980 [For some introductory references on multicomponent and multiphase sterns, see this reference and also see H. E. Stanley, Introduction to Phase Transitions and Critical Phenomena, Oxford University Press, New York, 1971.]... 

Narins, B., ed. 2001. World of Computer Science. Detroit Gale Group/Thomson Learning. (2 vols.) A good introductory reference on the subject with an impressive list of contributors and advisors. Alphabetically arranged, the 800+ entries discuss pioneers, discoveries, theories, concepts, issues, and ethics. Of particular interest are the biographies of living computer personalities. Not aimed at an academic audience. Choice remarks that it will help new computer science students and professionals alike. 

Light scattering is introduced and modelled for nematic liquid crystals in Section 5.10. Suitable introductory references to the literature on light scattering are also given. 

The introductory remarks about unimolecular reactions apply equivalently to bunolecular reactions in condensed phase. An essential additional phenomenon is the effect the solvent has on the rate of approach of reactants and the lifetime of the collision complex. In a dense fluid the rate of approach evidently is detennined by the mutual difhision coefficient of reactants under the given physical conditions. Once reactants have met, they are temporarily trapped in a solvent cage until they either difhisively separate again or react. It is conmron to refer to the pair of reactants trapped in the solvent cage as an encounter complex. If the unimolecular reaction of this encounter complex is much faster than diffiisive separation i.e., if the effective reaction barrier is sufficiently small or negligible, tlie rate of the overall bimolecular reaction is difhision controlled. 

Introductory text, fairly mathematical, concentrates on spin/ = systems, good references. 

Introductory descriptions of Hartree-Fock calculations [often using Rootaan s self-consistent field (SCF) method] focus on singlet systems for which all electron spins are paired. By assuming that the calculation is restricted to two electrons per occupied orbital, the computation can be done more efficiently. This is often referred to as a spin-restricted Hartree-Fock calculation or RHF. 

Oligonucleotide synthesis involves specialized blocking and coupling reactions the chemistry of which is beyond the scope of a typical introductory course The in terested reader is referred to http //WWW bi umist ac uk/ users/dberrisford/1 MBL/ nucleicacidB html... 

Two other techniques that depend only on base SI units are coulometry and isotope-dilution mass spectrometry. Coulometry is discussed in Chapter 11. Isotope-dilution mass spectroscopy is beyond the scope of an introductory text, however, the list of suggested readings includes a useful reference. 

R. E. Mausser, ed.. The Vanderbilt Eatex Handbook, 3rd ed., R. T. Vanderbilt Co., Inc., Norwalk, Conn., 1987. Contains introductory and reference information for people engaged in the latex branch of the mbber industry. 

References General (textbooks that cover at an introductory level a variety... 

The following books and reviews provide fuller details of the topics indicated in this chapter. The authors recommendations for excellent introductory and/or reference texts to the topics are indicated with. [For earlier bibliographies see Purification of Laboratory Chemicals, 4th Edn, ISBN 0750628391 (1996, hardback) and 0750637617 (1997, paperback). 

It is recommended at this stage of the text that the reader unfamiliar with the basic concepts of variation and process capability refer to Appendix I for an introductory treatise on statistics, and Appendix II for a discussion of process capability studies. 

The purpose of this subsection is to familiarize the reader with some of the basic characteristics and problems of composite laminate joints. The specific design of a joint is much too complex for an introductory textbook such as this. The published state-of-the-art of laminate joint design is summarized in the Structural Design Guide for Advanced Composite Applications [7-5] and Military Handbook 17A, Plastics for Aerospace Vehicles, Part 1, Reinforced Plastics [7-6]. Further developments can be found in the technical literature and revisions of the two preceding references. 

We close these introductory remarks with a few comments on the methods which are actually used to study these models. They will for the most part be mentioned only very briefly. In the rest of this chapter, we shall focus mainly on computer simulations. Even those will not be explained in detail, for the simple reason that the models are too different and the simulation methods too many. Rather, we refer the reader to the available textbooks on simulation methods, e.g.. Ref. 32-35, and discuss only a few technical aspects here. In the case of atomistically realistic models, simulations are indeed the only possible way to approach these systems. Idealized microscopic models have usually been explored extensively by mean field methods. Even those can become quite involved for complex models, especially for chain models. One particularly popular and successful method to deal with chain molecules has been the self-consistent field theory. In a nutshell, it treats chains as random walks in a position-dependent chemical potential, which depends in turn on the conformational distributions of the chains in... 

Introductory discussion of the scope and mechanism of each reaction has been kept to a minimum. Many excellent texts and reviews exist that provide thorough and accurate discussion of the more theoretical aspects of organic synthesis, and the student is referred to these sources and to the original literature frequently. Since it is the purpose... 

Introductory Remarks.—As a considerable amount of this material is likely to be known, we shall abridge the exposition, referring for details to the recent text of the author.6... 

Mass Spectra and Chemical Structure While there are a number of books (Refs 16, 30, 49 64) already referred to, which deal with details of the instrumentation and techniques of mass spectrometry, there are several concise introductory texts (Refs 10, 21 52) on the interpretation of mass spectra. Still other recent books deal comprehensively with organic structural investigation by mass spectrometry. One of these (Ref 63) discusses fundamentals of ion fragmentation mechanisms, while the others (Refs 7, 15, 20, 28 29) describe mass spectra of various classes of organic compounds. In the alloted space for this article methods of interpretation of mass spectra and structural identification can not be described in depth. An attempt is, therefore, made only to briefly outline the procedures used in this interpretation... 

The remainder of this introductory chapter covers a few general but important parameters of step-growth polymerization. References are provided throughout the chapter if further information is desired. Further details of specific polymers made by step-growth polymerization are provided in subsequent chapters within this book. 

The work of Melander and Carter (1964) on 2,2 -dibromo-4,4 -di-carboxybiphenyl-6,6 -d2 (1) has been referred to above in the introductory and theoretical sections, where it was pointed out that the availability of two detailed theoretical computations of the inversion barrier (Westheimer and Mayer, 1946, Westheimer, 1947 Hewlett, 1960) made this system especially attractive for the study of steric isotope efifects. Furthermore, in the preferred initial-state conformation the two bromines are probably in van der Waals contact (cf. Hampsoii and Weissberger, 1936 Bastiansen, 1950), and thus initial-state steric effects are unaffected by deuterium substitution in the 6 and 6 positions. The barrier calculations provided two different theoretical values for the non-bonded H Br distance in the transition state which, together with the corresponding H Br potential function, could be inserted in equation (10) to yield values for A AH. For... 

In this section, the characteristics of the spectra displayed by the different types of iron—sulfur centers are presented, with special emphasis on how they depend on the geometrical and electronic structure of the centers. The electronic structure is only briefly recalled here, however, and interested readers are referred to the excellent standard texts published on this topic (3, 4). Likewise, the relaxation properties of the centers are described, but the nature of the underlying spin-lattice relaxation processes is not analyzed in detail. However, a short outline of these processes is given in the Appendix. The aim of this introductory section is therefore mainly to describe the tools used in the practical applications presented in Sections III and IV. It ends in a discussion about some of the issues that may arise when EPR spectroscopy is used to identify iron-sulfur centers. 

The general theory of the quantum mechanical treatment of magnetic properties is far beyond the scope of this book. For details of the fundamental theory as well as on many technical aspects regarding the calculation of NMR parameters in the context of various quantum chemical techniques we refer the interested reader to the clear and competent discussion in the recent review by Helgaker, Jaszunski, and Ruud, 1999. These authors focus mainly on the Hartree-Fock and related correlated methods but briefly touch also on density functional theory. A more introductory exposition of the general aspects can be found in standard text books such as McWeeny, 1992, or Atkins and Friedman, 1997. As mentioned above we will in the following provide just a very general overview of this... 

Over 90 megabytes online of information on alchemy in all its facets. Divided into over 1300 sections and providing tens of thousands of pages of text, over 2000 images, over 200 complete alchemical texts, extensive bibliographical material on the printed books and manuscripts, numerous articles, introductory and general reference material on alchemy... 

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