Triazolate complexes copper

Relatively little has been reported on the electronic spectra of triazole and triazolate complexes. Copper(II) benzotriazolate adducts and benzotriazolate complexes show ligand-field maxima in the range 12.5-15.9 kK, in agreement with the proposed octahedral coordination geometry (172). Electronic spectra have also been reported for rhodium(I) and iridium(I) benzotriazolate complexes (33). 

Infrared data have been tabulated for benzotriazole and a wide range of its transition metal complexes or adducts (172). Far infrared spectra have been recorded for copper(II) benzotriazole adducts and bands at 270-320 cm-1 have been assigned to Cu-N vibrations (172). Infrared absorptions at approximately 825, 800, and 775 cm-1 in the spectra of cobalt(III)/4,5-disubstituted triazolate complexes have been attributed to triazolate ring vibrations (109). Infrared data have been reported and assignments made for palladium and platinum thiatriazoline-5-thionate complexes (37) and for the parent thione (127). Vibrational spectroscopy has been employed in an attempt to determine coordination sites for a range of 8-azapurine complexes (108). 

While the vast majority of reports describing the synthesis of triazoles used copper salts or discrete complexes to promote the reactions, a number of metal-free approaches have been developed. One example of this group used DBU in chloroform to effect the cycloaddition reaction (Scheme 3.109 and Example 3.15) [114,115]. A host of alkyl and... 

Click chemistry is now a popular concept, more specifically when it is used to indicate a copper-catalyzed cycloaddition reaction between alkyl or aryl azides and terminal alkynes. Due to the fact that Cu(I) catalysts dramatically accelerate the original Hiiisgen thermal reaction with perfect control of the mechanistic pathway to lead only to l,4-disubstituted-l,2,3-triazoles, the copper-catalyzed azide-alkyne cycloaddition (CuAAC) reaction has become one of the most representative examples of click chemistry. It was proposed that this reaction proceeds first through the formation of a copper(l)-acetyhde from a copper(I) catalyst and a terminal alkyne, followed by cycloaddition with a copper(l)-bound azide to generate a triazolyl copper(I) complex, which is released by protonation of the Cu—C bond. 

As part of efforts to develop novel, more efficient, OLEDs, Eisenberg and coworkers have generated the bidentate amine-1,2,3-triazole ligands, 53a-f, and used them to synthesize the heteroleptic copper(I) amido-1,2,3-triazole complexes... 

Fig. 10 The synthesis of heteroleptic copper amido-l,2,3-triazole complexes (54a-f) and the X-ray structure of the heteroleptic copper(I) amido-1,2,3-triazole complex, 54f [169]. Hydrogen atoms and counter ions have been omitted for clarity...

Azide-tagged copper(I) complexes of NHCs analogous to the well-known bis [2,6-diisopropylphenyl]imidazol-2-ylidene (IPr) and AfdV -bis[2,6-diisopropylphenyl] imidazolin-2-ylidene (SlPr) in the reaction with propargyl alcohols, yield triazole functionalized copper(l)-NHC complexes with 75% and 69% yield. This strategy opens the possibility of diversifying the substitution patterns of these copper(l) complexes (Scheme 3.2) [32]. 

In addition to bonding with the metal surface, triazoles bond with copper ions in solution. Thus dissolved copper represents a "demand" for triazole, which must be satisfied before surface filming can occur. Although the surface demand for triazole filming is generally negligible, copper corrosion products can consume a considerable amount of treatment chemical. Excessive chlorination will deactivate the triazoles and significantly increase copper corrosion rates. Due to all of these factors, treatment with triazoles is a complex process. 

Despite the weak basicity of isoxazoles, complexes of the parent methyl and phenyl derivatives with numerous metal ions such as copper, zinc, cobalt, etc. have been described (79AHC(25) 147). Many transition metal cations form complexes with Imidazoles the coordination number is four to six (70AHC(12)103). The chemistry of pyrazole complexes has been especially well studied and coordination compounds are known with thlazoles and 1,2,4-triazoles. Tetrazole anions also form good ligands for heavy metals (77AHC(21)323). 

The NHCs have been used as ligands of different metal catalysts (i.e. copper, nickel, gold, cobalt, palladium, rhodium) in a wide range of cycloaddition reactions such as [4-1-2] (see Section 5.6), [3h-2], [2h-2h-2] and others. These NHC-metal catalysts have allowed reactions to occur at lower temperature and pressure. Furthermore, some NHC-TM catalysts even promote previously unknown reactions. One of the most popular reactions to generate 1,2,3-triazoles is the 1,3-dipolar Huisgen cycloaddition (reaction between azides and alkynes) [8]. Lately, this [3h-2] cycloaddition reaction has been aided by different [Cu(NHC)JX complexes [9]. The reactions between electron-rich, electron-poor and/or hindered alkynes 16 and azides 17 in the presence of low NHC-copper 18-20 loadings (in some cases even ppm amounts were used) afforded the 1,2,3-triazoles 21 regioselectively (Scheme 5.5 Table 5.2). 

Finally, NHC complexes of copper, formed in situ from the hnidazolium salt and CuBr have been used in the monoarylation of aniline [167]. Trinuclear Cu(I) catalysts have been applied to the arylation of pyrazoles, triazoles, amides and phenols [168] (Scheme 6.50). 

Using a triazole-/pyrimidine-containing hybrid ligand, terminally coordinated in a thiocyanate-bridged copper(II) dimer, Haasnoot et al. reported250 the structure of the f3 isomer of complex (288), revealing that the Cu-SCN distance is relatively short compared to other Cu-SCN... 

The IR and Raman spectra of benzotriazole, benzotriazole anion and its Cu(I) complex have been measured. The characteristic peaks in the IR spectrum of the triazole moiety in benzotriazole anion occur at 1163 cm , 1134 cm , and 1115 cm . A broad band with a main peak at 1151 cm occurs in the spectrum of the Cu(I)-BTA complex <85JST(l00)57i>. The chemisorption of benzotriazole on clean copper and cuprous oxide surfaces is investigated by combining XPS, UV-PE and IR reflection absorption spectroscopy (IRAS). Coordination geometry including the triazole-... 

A plethora of crown ether- or cryptand type molecules have been reported. Some of them are depicted below to show their diversity and versatility. Lariat azaether containing cyclen macrocycle 208 [36] and azaethers involving triazole 209 [37], furane or pyrrole containing macrocycles which can complex two copper 210 [38] or one barium cations 211 [39], spiro-linked crown ethers 212 [40] andcagecompounds 213 [41] which, in addition to two alkali cations, could... 

Involvement of two nucleophilic nitrogen atoms is thus typical for the amino heterocycles. The mutual disposition of the pyridine and amine nitrogen atoms allows the formation of chelate structures for the cobalt complexes of purine, 221 and 222. Structures with the N, iV -five-membered metal cycles were proven for the tri- and tetranuclear complexes of silver ) with 8-aminoquinoline (223) (92IC4370), and polymeric copper- and rhodium-acetate clusters (224). Another coordination mode can be found in the complexes of 4-amino-3,5-bis(pyridin-2-yl)-l,2,4-triazole, (225 or... 

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