Structural systematics

Intermediates involved in the tautomerization of furoxans gave rise to speculations about their structure. Systematic calculations on possible intermediates being involved in the reaction of furoxan [92JCC177] and benzofuroxan 79 showed that dinitrosoethylene and dinitrosobenzene 81 are the most likely ones (Scheme 50) [94JOC6431, 94JPC12933]. 

Structural systematics in actinide fluoride complexes. R. A. Permman, R. R. Ryan and A. Rosen-zweig, Struct. Bonding (Berlin), 1973,13,1-52 (174). 

Penneman RA, Ryan RR, Rosenzweig A (1973) Structural Systematics in Actinide Fluoride Complexes. 13 1-52... 

Structural systematics of 1,1-1,2-dithiolato chelates Dithiolene chelates... 

Although Ni(CO)4 was discovered many years ago, no neutral Ni2(CO)x compound has ever been synthesized in macroscopic amounts. However, several communications report ionic species such as [Ni2(CO)8l+, [Ni2(CO)7], and [Ni2(CO)6]+, where structures with one or two bridging carbonyls are proposed.2418 Plausible structures for neutral Ni2(CO)x (x = 5, 6, 7) have been investigated by theoretical methods, and decomposition temperatures well below room temperature have been predicted.2419,2420 Tetra-, penta-, and hexanuclear nickel carbonyl clusters have been investigated by means of molecular orbital theory. It is found that the neutral forms are more stable than the corresponding anionic forms but the anionic forms gain in stability as the nuclearity rises.2421 Nickel carbonyl cluster anions are manifold, and structural systematics have been reviewed.2422,2423 An example includes the anion [Ni9(CO)i6]2- with a close-packed two-layer metal core.2424... 

See also Carboranes structural systematics, 4 172-179 weakest anions and strongest acids, 4 202-204... 

Metalloboranes, 4 172 exopolyhedral, 4 208-210 main group element, 4 207-208 transition element, 4 205-207 Metallo-carbohedrene clusters, 4 648 Metallocarboranes, 4 170 as catalysts, 4 217-218 economic aspects, 4 229 exopolyhedral, 4 215-216 f-block element, 4 225-226 host-guest chemistry-carborane anticrowns, 4 216-217 structural systematics, 4 176-179 transition metal, 4 210-215 Metallocene catalysis, MAO in, 16 92-93. 

Management system Structured, systematic method to implement an identified set of activities with assigned responsibilities and accountability. 

The basic aspects of the structural systematic and the chemical bonding are discussed as well as ambiguous topological aspects and selected physical properties (magnetism, conductivity) of the respective alloys. 

For example, both Hiickel aromatics B and C conform to the Wade-Mingos electron counting rules [2] (see Chapter 1.1.2) and to the structural systematics developed for boranes and heteroboranes [1] the hexagonal bipyramid with the apices removed is in agreement with an arachno electron count of 18 SE for (CH)g [2],... 

In this chapter, general aspects and structural properties of crystalline solid phases are described, and a short introduction is given to modulated and quasicrystal structures (quasi-periodic crystals). Elements of structure systematics with the description of a number of structure types are presented in the subsequent Chapter 7. Finally, both in this chapter and in Chapter 6, dedicated to preparation techniques, characteristic features of typical metastable phases are considered with attention to amorphous and glassy alloys. 

Identifying and analyzing fire hazards and scenarios is the next step in a fire risk assessment. The hazard identification should be structured, systematic, audit-able, and address all fire hazards, including nonprocess fires. The result of the hazard identification is a list of potential fire hazards that may occur at the facility, for example, jet, pool, flash, BLEVE, electrical, or Class A fires. This list should also include the location where each fire could occur. Hazard identification techniques used to identify potential hazards are shown in Table 6-1. 

Structure Systematic name lUPAC approved name... 

A considerable number of clusters with more than six metal atoms has been prepared. There is no structural systematics for these yet, but in one case of a Rhjg-clus-ter (72) it has been shown that the packing of metal atoms in a big cluster can be the same as that of a closely packed array in the pure metal. In the following structural drawings all ligands are omitted to allow a clear view of the metal atom arrangement. 

We shall prepare the various building blocks of the catalyst surface and study them separately. Then we put the parts together and the resultant structure should have all of the properties of the working catalyst particle. Just as in the case of synthetic insulin or the B12 molecule, the proof that the synthesis was successful is in the identical performance of the synthesized and natural products. Our building blocks are crystal surfaces with well-characterized atomic surface structure and composition. Cutting these crystals in various directions permits us to vary their surface structure systematically and to study the chemical reactivity associated with each surface structure. If we do it properly, all of the surface sites and microstructures with unique chemical activity can be identified this way. Then, by preparing a surface where all of these sites are simultaneously present in the correct configurations and concentrations the chemical behavior of the catalyst particle can be reproduced. The real value of this synthetic approach is that ultimately one should be able to synthesize a catalyst that is much more selective since we build into it only the desirable active sites in a controlled manner. 

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