Interest coverage

CA now systematically covers more than 9000 journals. We are sometimes asked what determines whether or not a journal is covered. The answer is that a journal is regularly examined as soon as it is discovered that at least occasionally it contains new information of chemical interest. Coverage, of course, does not mean abstracting all papers in a journal. As a matter of fact, CA abstracts all papers of only a comparatively small percentage of the journals in the List of Periodicals Abstracted by Chemical Abstracts (those devoted strictly to original papers in the field of chemistry). The above criteria for inclusion are applied to individual papers, not to journals. Many trade journals are covered, as well as... 

The waterfall process for interest payments is shown at Exhibit 15.7. Before paying the next priority of the waterfall, the vehicle must pass a number of compliance tests designed to measure the overall robustness of cash flow being generated by the collateral portfolio. These metrics include tests such as interest coverage and principal (par) coverage, which is similar in concept to bank loan covenants and explained more fully later. 

Interest coverage the level of net interest income on the portfolio (i.e., after defaults) must be sufficient to cover interest due on the liabilities. 

This book gives an excellent introduction to many of the best ideas from the field of automatic programming, an interesting coverage of some new ideas developed by the author, and a description of an ambitious synthesis system that utilizes them for practical automatic program synthesis. 

Infrared Spectroscopy. The infrared spectroscopy of adsorbates has been studied for many years, especially for chemisorbed species (see Section XVIII-2C). In the case of physisorption, where the molecule remains intact, one is interested in how the molecular symmetry is altered on adsorption. Perhaps the conceptually simplest case is that of H2 on NaCl(lOO). Being homo-polar, Ha by itself has no allowed vibrational absorption (except for some weak collision-induced transitions) but when adsorbed, the reduced symmetry allows a vibrational spectrum to be observed. Fig. XVII-16 shows the infrared spectrum at 30 K for various degrees of monolayer coverage [96] (the adsorption is Langmuirian with half-coverage at about 10 atm). The bands labeled sf are for transitions of H2 on a smooth face and are from the 7 = 0 and J = 1 rotational states Q /fR) is assigned as a combination band. The bands labeled... 

We now consider how one extracts quantitative infonnation about die surface or interface adsorbate coverage from such SHG data. In many circumstances, it is possible to adopt a purely phenomenological approach one calibrates the nonlinear response as a fiinction of surface coverage in a preliminary set of experiments and then makes use of this calibration in subsequent investigations. Such an approach may, for example, be appropriate for studies of adsorption kinetics where the interest lies in die temporal evolution of the surface adsorbate density N. ... 

The Langmuir equation is based on the assumption that the heat of adsorption does not vary with the coverage 6 it is interesting that in the systems just quoted, the heat of adsorption varies with the amount adsorbed in the case of CO, but is virtually constant in the case of Ar. 

Additional discussions are available in the General References concerning the properties of several nitrofiirans. This includes further coverage of the chemotherapeutic and physical properties antimicrobial activity bacterial resistance absorption, distribution, and excretion clinical use and safety studies, of this interesting class of antiinfective compounds. 

Metal Ion-Promoted Reactions of Thiols. Metal ion-promoted reactions of thiols have been reviewed (53). The bulk of the coverage concerns metal ion promoted aspects of sulfur chemistry. The main topics of interest are the formation of sulfenamides, sulfides, and disulfides using metal-mediated reactions. 

An interesting field of application is the protection of tantalum against hydrogen embrittlement by electrical connection to platinum metals. The reduction in hydrogen overvoltage and the shift of the free corrosion potential to more positive values apparently leads to a reduced coverage by adsorbed hydrogen and thereby lower absorption [43] (see Sections 2.1 and 2.3.4). 

We sometimes kept certain information contained in a particular author s work even though the same topic is given partial coverage elsewhere in this book. We tried to remember that we wanted to achieve technical relevance, readability, and balance. Occasionally, we decided that the inclusion of a parallel text offered a different or additional perspective, perhaps with new or different illustrations, or an interesting but straightforward matliematical treatment. 

Thousands of technical papers and many books have been written on the subject of phenolic resins. The polymer is used in hundreds of diverse applications and in very large volumes. It is used worldwide. In fact the term phenolic resin encompasses a wide variety of materials based on a broad range of phenols and co-monomers. In this short article, we cannot expect complete coverage. Our hope is that we can provide an understanding of the fundamental chemistries, uses, and values of these materials as well as enough references to permit the interested reader to begin his own exploration of the topic. 

Part Three is intended to balance the coverage of Parts One and Two and to serve as a convenient guide to the now enormous literature of multistep synthesis. Information on more than five hundred interesting multistep syntheses of biologically derived molecules is included. It is hoped that the structural range and variety of target molecules presented in Part Three will appeal to many chemists. 

In the last decade two-dimensional (2D) layers at surfaces have become an interesting field of research [13-27]. Many experimental studies of molecular adsorption have been done on metals [28-40], graphite [41-46], and other substrates [47-58]. The adsorbate particles experience intermolecular forces as well as forces due to the surface. The structure of the adsorbate is determined by the interplay of these forces as well as by the coverage (density of the adsorbate) and the temperature and pressure of the system. In consequence a variety of superstructures on the surfaces have been found experimentally [47-58], a typical example being the a/3 x a/3- structure of adsorbates on a graphite structure (see Fig. 1). 

In this review we consider several systems in detail, ranging from idealized models for adsorbates with purely repulsive interactions to the adsorption of spherical particles (noble gases) and/or (nearly) ellipsoidal molecules (N2, CO). Of particular interest are the stable phases in monolayers and the phase transitions between these phases when the coverage and temperature in the system are varied. Most of the phase transitions in these systems occur at fairly low temperatures, and for many aspects of the behavior quantum effects need to be considered. For several other theoretical studies of adsorbed layer phenomena see Refs. 59-89. 

The literature in this area is extensive and some of the concepts and symbolism may be transitory. This chapter reviews the field at a level and with a coverage adequate for the experimentalist to use the standard relationships and to follow their use in the mechanistic literature. Research on the meaning of the extrathermody-namic relationships themselves is beyond our needs the interested reader can explore these ideas further in the references cited. Grunwald has reviewed the early history of LFERs. 

Chemical reduction is used extensively nowadays for the deposition of nickel or copper as the first stage in the electroplating of plastics. The most widely used plastic as a basis for electroplating is acrylonitrile-butadiene-styrene co-polymer (ABS). Immersion of the plastic in a chromic acid-sulphuric acid mixture causes the butadiene particles to be attacked and oxidised, whilst making the material hydrophilic at the same time. The activation process which follows is necessary to enable the subsequent electroless nickel or copper to be deposited, since this will only take place in the presence of certain catalytic metals (especially silver and palladium), which are adsorbed on to the surface of the plastic. The adsorbed metallic film is produced by a prior immersion in a stannous chloride solution, which reduces the palladium or silver ions to the metallic state. The solutions mostly employed are acid palladium chloride or ammoniacal silver nitrate. The etched plastic can also be immersed first in acidified palladium chloride and then in an alkylamine borane, which likewise form metallic palladium catalytic nuclei. Colloidal copper catalysts are of some interest, as they are cheaper and are also claimed to promote better coverage of electroless copper. 

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