Derivatives complexation

In the European Union, coal-derived complex chemical substances, ie, those contained in the European Inventory of Existing Commercial Chemical Substances, have been classified for carcinogenicity in the twenty-first adaptation to technical progress of the European Commission (EC) Dangerous Substances Directive 1994 67/548/EEC (57). The EC Regulation 793/93 requires data sets to be submitted by producers or importers to the... 

Partially dehydrated derivatives complexed with polyethylene glycol or propylene glycol exist. In the United of hydration has been replaced by glycine are particularly popular. Aluminum zirconium tetrachlorhydrex gly antiperspinant products. 

Although Lehn and his coworkers prepared a large number of cryptands and derived complexes over the years, the synthetic approach to these compounds remained essentially similar for most of them. Details are presented for a number of such compounds in ref. 26. The essential features of these syntheses were use of amide-forming reactions in the absence of templating ions with reliance on a high dilution step to form the second ring. An alternative approach for the synthesis of cryptands was developed by Dye and his coworkers. Their approach involved the use of a flow synthesis to replace the high dilution step. 

Chiral boron(III) complexes can catalyze the cycloaddition reaction of glyoxy-lates with Danishefsky s diene (Scheme 4.18) [27]. Two classes of chiral boron catalyst were tested, the / -amino alcohol-derived complex 18 and bis-sulfonamide complexes. The former catalyst gave the best results for the reaction of methyl glyoxylate 4b with diene 2a the cycloaddition product 6b was isolated in 69% yield and 94% ee, while the chiral bis-sulfonamide boron complex resulted in only... 

Most of the inhibitors in use are organic nitrogen compounds and these have been classified by Bregman as (a) aliphatic fatty acid derivatives, b) imidazolines, (c) quaternaries, (d) rosin derivatives (complex amine mixtures based on abietic acid) all of these will tend to have long-chain hydrocarbons, e.g. CigH, as part of the structure, (e) petroleum sulphonic acid salts of long-chain diamines (preferred to the diamines), (/) other salts of diamines and (g) fatty amides of aliphatic diamines. Actual compounds in use in classes (a) to d) include oleic and naphthenic acid salts of n-tallowpropylenediamine diamines RNH(CH2) NH2 in which R is a carbon chain of 8-22 atoms and x = 2-10 and reaction products of diamines with acids from the partial oxidation of liquid hydrocarbons. Attention has also been drawn to polyethoxylated compounds in which the water solubility can be controlled by the amount of ethylene oxide added to the molecule. 

Acetic add, ethylenediaminetetra-, 4,253 add-base equilibria, 2,779 in analysis, 1,522 complexes composition, 2,783 coordination numbers, 2,783 solid state structure, 2,783 cyclic derivatives complexes, 2,785 in electroplating, 6,14 heteroatom derivatives metal complexes, 2, 786 homologs... 

The reaction of alkenylcarbene complexes and imines in the presence of a Lewis acid generates pyrroline derivatives as a result of a [3C+2S] cyclisation process [76]. This reaction has been extended to an asymmetric version by the use of chiral alkenylcarbene complexes derived from several chiral alcohols. However, the best results are found when (-)-8-phenylmenthol-derived complexes are used and catalytic amounts of Sn(OTf)2 are added to the reaction. In these conditions high levels of trans/cis selectivity are achieved and the hydrolysis of the major tram diastereoisomers allows the preparation of optically pure 2,5-disubstituted-3-pyrrolidinone derivatives (Scheme 29). 

Tungsten alkynyl Fischer carbene complexes are excellent dienophile partners in the classical Diels-Alder reaction with 1-azadienes (see Sect. 2.9.2.1). On the contrary, the chromium-derived complexes exhibit a different behaviour and they react through a [4S+3C] heterocyclisation reaction to furnish azepine derivatives [116] (Scheme 68). The reaction is initiated by a 1,2-addition of the nitrogen lone pair to the carbene carbon followed by a [l,2]-Cr(CO)5 shift-pro-... 

The following order of initiation rate constants was found by Grubbs et al. for 71a and some precatalysts containing one phosphine ligand 56d< 56k 71a<56h (cf. Scheme 15 for structures of 56d,h,k) [48b, 55]. Thus, 71a shows a rate of initiation comparable to that of 56k but three orders of magnitude higher than that of 56d. Nevertheless, 56d appears to be more reactive in RCM reactions than 71a [56]. Wakamatsu and Blechert were the first to report that the activity of precatalysts related to 71a can be dramatically enhanced by modification of the benzylidene unit [56]. For example, RCM of 75 using 1 mol% of BINOL-derived complex 71b yields the azacyclic product 76 in quantitative yield within 20 min (Eq. 10), whereas with 56d only 4% of 76 was obtained under these conditions [56]. 

Dihydro-l,2,5-thiadiboroles (Et2C2B2R2S) have remarkable acceptor properties toward metal-ligand moieties. Dihydrothiadiborole-derived complexes can be achieved thermally or photochemically, e.g., Co and Fe sandwich, triple-decked and even tetradecked complexes are known, all having direct metal-boron bonds. 

Laube and Hollenstein [21, 61] studied the single crystal structures of cyclohexanone derivatives complexed with a Lewis acid and found pyramidalization of the carbonyl carbon (4, Fig. 4), in agreement with the observed selectivity [61]. 

Cronje, S., Raubenheimer, H.G., Spies, H.S.C., Esterhuysen, C., Schmidbaur, H., Schier, A. and Kruger, G.J. (2003) Synthesis and characterisation of N-coordinated pentafluorophenyl gold(I) thiazole-derived complexes and an unusual self-assembly to form a tetrameric gold(I) complex. Dalton Transactions, (14), 2859-2866. 

Complex stability constants are most often determined by pH-potentiometric titration of the ligand in the presence and absence of the metal ion.100 This method works well when equilibrium is reached rapidly (within a few minutes), which is usually the case for linear ligands. For macrocyclic compounds, such as DOTA and its derivatives, complex formation is very slow, especially for low pH values where the formation is not complete, therefore a batch method is... 

Following the generation of a macrocyclic ring by a template reaction it has often been the practice to modify the ring by further reaction. Examples of such modification are given by the formation of the derivative complexes (71) and (72) discussed in Section 2.3. Other examples are described in subsequent chapters - in particular, ligand redox reactions have been widely used and a range of such reactions is presented in Chapter 8. 

In the case of DTPA derivative complexes, both proton- and metal-assisted (Zn2+ or Cu2+) pathways are important for the dissociation (143). For the DTPA-amide derivatives, the proton-assisted dissociation is much faster, while the metal-assisted pathway is slower (147,148), with a dependency of the... 

Beside changes in the rotational correlation time, modifications in the hydration state of the chelate were also used to follow enzymatic activity. Gd(HP-D03A)-derivative complexes bearing a galactopyranose moiety were studied as reporters for... 

Starting from 2,4,6-octatriene and pivaldehyde, the conjugated homoallylic alcohol 8 is obtained as the sole product. Cycloheptatriene-derived complexes react with aldehydes and C02 to afford mixtures of the isomeric 1,3- and 1,4-cycloheptadienyl carbinols or acids, respectively. Interestingly, analogous reactions with methyl chloroformate or dimethyl carbamoyl chloride produce the conjugated dienyl ester 9 or amide 10 as unique products [19,20]. 

Bis(oxazoline)-copper complexes supported on clays were investigated as heterogeneous catalysts in the cyclopropanation reaction (37, 38). Optimal results were obtained from chloride-derived complexes in nitroethane as reaction medium. Laponite clay was found to provide higher selectivities than montmorillonite or bentonite. In every case, the heterogeneous reaction afforded increased amounts of the cis cyclopropane relative to the homogeneous reaction. 

Table 8.1 compiles the most common stable homonuclear neutral binary carbonyls. They can be prepared by direct carbonylation of pure metals or made from available metallic precursors by reductive carbonylation. However, most of them are commercially available. Moreover, heteronuclear carbonyl compounds are known, and they are usually prepared by reaction between homonuclear binary carbonyls or carbonyl-derivative complexes. 

Ruthenium catalysts prepared from Ru3(CO)i2 and other related carbonyl-derived complexes have been widely used in reactions of hydrogenolysis, homologation and dimerization of alkanes [114—116]. Catalysts derived from carbonyl precursors usually show higher catalytic activities than conventionally prepared supported mthenium catalysts. This correlates well with the smaller crystallite size achieved by using carbonyl precursors. 

The use of naturally derived complex carbon compounds as raw materials for polyurethane polymers is not new to the industry. Since the advent of polyether polyols, polyurethane polymers have utilized natural sources of renewable carbon. 

Scheme 4.14 Amino acid receptors developed by Kim, Chin, and co-workers. D-Amino acids are favored as a result of steric strain present in the L-amino acid-derived complex [97].

Diazasilacyclopent-4-ene derivatives complexed with palladium and copper halides (Section 4.24.1.3.4.) (cf. (27)) possess UV absorption at 436-655 nm range <86ZN(B)1230>. 

A detailed examination of OSO4 reactions with A -steroids has been reported." The A-ring conformation of the reactant or derived complex is important in determining the stereoselectivity of these reactions, and the major role of the proximate substituents is to anchor the appropriate conformation favouring a- or /3-attack. Studies on the stereochemistry of electrophilic attack on cholest-5-en-3-one continue." As with bromine chloride," appreciable /3-attack occurs and the 5/3,6j8-epoxide was isolated along with the previously reported 5a,6a-epoxide and the Baeyer-Villiger product, the A-homo-enol lactone (58). Base-catalysed... 

In 1991, Evans and co-workers employed CuOTf-derived complexes of bis-(oxazoline) ligands 2, 3, 7b, 38, and 45 in the same cyclopropanation reaction of... 

Diels-Alder reaction of furan 90 and 3-acrylol-l,3-oxazolidin-2-one 69 was effectively carried out with Cu(ll)-bu-box 3-derived complex. The corresponding... 

Pyrazolate-based dinucleating hgands have proven useful to control crucial characteristics of the dicopper core, such as the Cu - Cu separation and the electronic properties of the metal ions, by variation of the chelate side arms attached to the heterocycle (31). This leads to greatly differing activities in the catalytic oxidation of DTBC mediated by those dicopper complexes [133,135]. While most of the pyrazolate-derived complexes 31 display an enzyme-hke Michaehs-Menten type kinetic behavior, it is apparent that both the Cu - Cu separation as well as the redox potential play an important... 

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