Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Complex-type

In general, little use is made in the process industry of more sophisticated approaches such as job and task analysis (see Chapter 4) to define the mental and physical skills required for specific types of work, and to tailor the training program accordingly. Instead, informal on-the-job training is common, even in more complex types of work such as control room tasks. Although the necessary skills will eventually be acquired by this process, its inefficiency... [Pg.130]

Complex type 02 M ratio Structure (i(0-0)/pm (normal range) u(0-0)/cm (normal range)... [Pg.617]

It should be pointed out that the existence of stable structures of the intermediate-complex type (also known as a-complexes or Wheland complexes) is not of itself evidence for their being obligate intermediates in aromatic nucleophilic substitution. The lack of an element effect is suggested, but not established as in benzene derivatives (see Sections I,D,2 and II, D). The activated order of halogen reactivity F > Cl Br I has been observed in quantita-tivei36a,i37 Tables II, VII-XIII) and in many qualitative studies (see Section II, D). The reverse sequence applies to some less-activated compounds such as 3-halopyridines, but not in general.Bimolecular kinetics has been established by Chapman and others (Sections III, A and IV, A) for various reactions. [Pg.170]

The composition of these alloys extends beyond the binary system and they may be categorised as the Duralumin type H15 and the complex types H12 and H16. [Pg.657]

Uniform rates of corrosion such as general etch corrosion seldom occur in steam-water circuits. Rather, pitting, tuberculation, and other complex types of corrosion tend to predominate. These forms of corrosion often result directly or indirectly from reactions occurring in particular areas of the system where fouling and deposition may be present. [Pg.153]

The most complex type of gas-liquid-particle process is one in which gaseous components participate in a heterogeneous catalytic reaction, with the formation of gaseous products. The following elementary steps must occur in a process of this type ... [Pg.82]

This index contains over 25 000 entries to the 6562 text pages of Volumes 1-6. The index covers general types of coordination complex, specific coordination complexes, general and specific organic compounds where their synthesis or use involves coordination complexes, types of reaction (insertion, oxidative addition, etc.), spectroscopic techniques (NMR, IR, etc.), and other topics involving coordination complexes, such as medicinal and industrial applications. [Pg.73]

For clarity, the reactions contained in this section can be divided into three categories according to the structure of the carbene complexes (Fig. 4) (i) those in which the dienophile and the diene are tethered through the heteroatom and the carbene carbon of the complex (type 1), (ii) those in which the dienophile and the diene are part of the same carbon chain (type 2), and finally (iii) those where the diene and the dienophile belong to different ligands within the complex (type 3). [Pg.99]

The H—NMR spectra indicate displacements of chemical shifts for the double bond protons of MA and TBSM and protons of the CH2—Sn group which suggest that two complex types are present in the mixture of the monomer pairs under study ... [Pg.113]

Fig. 3. Rapid Mo(V) EPR signals obtained on reducing xanthine oxidase at pH 10 with 15 moles of xanthine for 1 min. at about 20 °. The upper four spectra are at 9.1 GHz and the lower four at 34.4 GHz. a, a, c, 8 refer to H2O as solvent and b, b, d, d to D2O. a, b, c, d are computer simulations of the experimental spectra, a, b, c, d, respectively. The interpretation is that two species, each having exchangeable protons which interact with Mo(V), are responsible for the signals. For one of these (dotted complex type II) there are two equivalent interacting protons and for the other (dashed complex type I), two non-equivalent protons. These species are believed to correspond to two different complexes of reduced xanthine oxidase with xanthine. (Reproduced from ref. 78 see also Table 2 for the parameters of the signals.)... Fig. 3. Rapid Mo(V) EPR signals obtained on reducing xanthine oxidase at pH 10 with 15 moles of xanthine for 1 min. at about 20 °. The upper four spectra are at 9.1 GHz and the lower four at 34.4 GHz. a, a, c, 8 refer to H2O as solvent and b, b, d, d to D2O. a, b, c, d are computer simulations of the experimental spectra, a, b, c, d, respectively. The interpretation is that two species, each having exchangeable protons which interact with Mo(V), are responsible for the signals. For one of these (dotted complex type II) there are two equivalent interacting protons and for the other (dashed complex type I), two non-equivalent protons. These species are believed to correspond to two different complexes of reduced xanthine oxidase with xanthine. (Reproduced from ref. 78 see also Table 2 for the parameters of the signals.)...
We have considerable latitude when it comes to choosing the chemical composition of rubber toughened polystyrene. Suitable unsaturated rubbers include styrene-butadiene copolymers, cis 1,4 polybutadiene, and ethylene-propylene-diene copolymers. Acrylonitrile-butadiene-styrene is a more complex type of block copolymer. It is made by swelling polybutadiene with styrene and acrylonitrile, then initiating copolymerization. This typically takes place in an emulsion polymerization process. [Pg.336]

Levelling acid dyes and particularly 1 1 metal-complex types generally require an exceptionally low pH in order to promote exhaustion and levelling up to 3% o.w.f. sulphuric acid is most commonly used for levelling acid dyes, although hydrochloric, formic and phosphoric acids are also effective. In the case of conventional 1 1 metal-complex dyes it is essential to use a sufficient excess of acid over and above the typical 4% o.w.f. sulphuric acid normally absorbed by the wool, otherwise there may be a tendency towards tippy dyeings and lower wet fastness. The actual excess required depends on applied depth and liquor ratio [2] typical recommendations are given in Table 12.2. [Pg.351]

A fourth family of A-glycans are referred to as hybrid glycans. These glycans share structural features of the high mannose and complex-type families. They usually retain two mannoses on the 6-arm of the trimannosyl core whilst complex-type antennae are elaborated on the 3-arm. Hybrid structures are frequentiy bisected and may also be core fucosylated (Fig. 15.1). It should be noted that whilst core fucosylation is common in complex-type, hybrid and truncated glycans, it is rarely found in high mannose glycans. [Pg.297]


See other pages where Complex-type is mentioned: [Pg.103]    [Pg.312]    [Pg.375]    [Pg.290]    [Pg.156]    [Pg.158]    [Pg.309]    [Pg.531]    [Pg.248]    [Pg.100]    [Pg.119]    [Pg.135]    [Pg.176]    [Pg.76]    [Pg.225]    [Pg.226]    [Pg.521]    [Pg.521]    [Pg.521]    [Pg.180]    [Pg.184]    [Pg.254]    [Pg.176]    [Pg.103]    [Pg.74]    [Pg.693]    [Pg.17]    [Pg.327]    [Pg.329]    [Pg.1222]    [Pg.181]    [Pg.238]    [Pg.352]    [Pg.353]    [Pg.355]    [Pg.309]    [Pg.295]    [Pg.297]   
See also in sourсe #XX -- [ Pg.441 , Pg.444 ]




SEARCH



Alkene metathesis Grubbs-type” complexes

Alkene metathesis Hoveyda-type” complexes

Alkylidene complexes Schrock-type

Alkylidyne-metal complexes Fischer-type

Aluminium complexes salen-type

Azomethine-type complex salts

Benzenoid Type Complexes

Cage-type packing structure, inclusion complexes

Cage-type structures cyclodextrin complexes

Carbohydrates, complex types

Catalytic hydrogenation, Ziegler-type complexes

Catalytic metathesis Hoveyda-type complexes

Channel-type complexes

Chiral Complexes of the and Types

Cobalt hydride complexes carbonyl type

Complex allyl-type

Complex light types

Complex perovskite-type oxide

Complex type lacdiNAc pathway

Complex type oligosaccharides

Complex type terminal reactions

Complex-type /V-glycans

Complexed lithium amides structural types

Complexes coordination-type nomenclature

Complexes neopentyl-type

Complexes of the Type M(AA)

Complexes of the Type M(L)

Complexes of the type

Complexes pyrazole-type ligands

Complexes sandwich-type

Compound-type complex oxides

Container Molecules Host Systems and Complex Types

Copper complexes center types

Crabtree-type complexes

Cyclopentadienyl complexes ansa type

Cyclopentadienyl-type ruthenium complexes

Diastereoisomers complex types

Elution Order in the -Type Complexes

Fischer-type carbene complexes

Fischer-type carbenes transition metal complexes

Fischer-type chromium carbene complexes

Fischer-type complexes

Formation and Structure of Pendant-Type Polymer-Metal Complexes

Formation of complex-type

Further Terminal Reactions in Complex-Type Oligosaccharide Synthesis

Grubbs-type complexes

Hoveyda - Grubbs type complex

Hoveyda-type complexes

Hydrosulfido complexes types

Influence of Polymer Type on Complex Properties

Iron hydride complexes carbonyl type

Katsuki-type complexes

Lantern-type complexes

Layer-type cyclodextrin complexes

Lead complexes sandwich-type

Lewis-type complexes

Metal carbene complexes Fischer-type

Metal complex types

Metal complex types carbyne

Metal complex types spectrochemical series

Metal complexes, donor-type

Methanide-type complexes

Molybdenum complexes Schrock-type

Novel Variant Pathways in Complex-type Oligosaccharide Synthesis

Numbers, types complex

Occurrence of bond type in organo-transition metal complexes

Octahedral-type complexes

Onion-type complexes

Paddlewheel-type complexes

Pincer-Type Iridium Complexes for Organic Transformations

Pincer-type complexes

Pincer-type complexes applications

Pincer-type complexes chiral

Pincer-type complexes preparation

Pincer-type complexes structure

Polynuclear complexes mixed valence type

Rare Earth Complexes with Aliphatic Amide Type Ligands

Rare Earth Complexes with Imidazole Type Ligands

Rare Earth Complexes with Imine Type Ligands

Rare Earth Complexes with N-Heterocyclic Type Ligands

Rare Earth Complexes with Phthalocyanine Type Ligands

Rare Earth Complexes with Porphyrin Type Ligands

Rare Earth Complexes with Pyridine Type Ligands

Rare Earth Complexes with Silyl Amide Type Ligands

Rhodium complexes pincer-type

Schrock-type alkylidyne complexes

Schrock-type alkylidyne-metal complexes

Schrock-type carbene complexes

Schrock-type carbene complexes, transition metal

Schrock-type complexes

Sellmann-type metal complexes

Slater type orbitals complex form

Sulfide complexes types

The Complexes—Types of Bonding

The LacdiNAc Pathway of Complex-Type Oligosaccharide Synthesis

The most important types of complexes applied in qualitative analysis

Three WERNER TYPE METAL COMPLEXES

Trisaccharides, complex-type

Type 11(G) Dioxygen Complexes

Type I Dioxygen Complexes

Type II polymers with pendant metal complexes

Type II(P) Dioxygen Complexes

Types of CD Observed for Cyclodextrin Complexes

Types of Complex Formed

Types of Cyclopentadienyl Complexes

Types of Heteroaromatic Ligands and Their Complexes

Types of Ligands and Complexes

Types of Luminescent Rare Earth Complexes for Bioimaging

Types of Metal Carbonyl Complexes

Types of complex reactions

V-type complexes

Vaska-type complex

Vaska-type rhodium complexes

Wemer-type complex

Werner-type complexes

Werner-type coordination complexes

Wilkinson type complex

Ziegler-type complexes, catalytic

© 2019 chempedia.info