The synthesis, complete characterization, and solid state structural and solution conformation determination of calix[n]arenes (n = 4, 6, 8) is reported. A complete series of X-ray structures of the alkali metal salts of calix[4]arene (HC4) illustrate the great influence of the alkali metal ion on the solid state structure of calixanions (e.g., the Li salt of monoanionic HC4 is a monomer; the Na salt of monoanionic HC4 forms a dimer; and the K, Rb, and Cs salts exist in polymeric forms). Solution NMR spectra of alkali metal salts of monoanionic calix[4]arenes indicate that they have the cone conformation in solution. Variable-temperature NMR spectra of salts HC4.M (M = Li, Na, K, Rb, Cs) show that they possess similar coalescence temperatures, all higher than that of HC4. Due to steric hindrance from tert-butyl groups in the para position of p-tert-butylcalix[4]arene (Bu(t)C4), the alkali metal salts of monoanionic Bu(t)C4 exist in monomeric or dimeric form in the solid state. Calix[6]arene (HC6) and p-tert-butylcalix[6]arene (Bu(t)C6) were treated with a 2:1 molar ratio of M(2)CO(3) (M = K, Rb, Cs) or a 1:1 molar ratio of MOC(CH(3))(3) (M = Li, Na) to give calix[6]arene monoanions, but calix[6]arenes react in a 1:1 molar ratio with M(2)CO(3) (M = K, Rb, Cs) to afford calix[6]arene dianions. Calix[8]arene (HC8) and p-tert-butylcalix[8]arene (Bu(t)()C8) have similar reactivity. The alkali metal salts of monoanionic calix[6]arenes are more conformationally flexible than the alkali metal salts of dianionic calix[6]arenes, which has been shown by their solution NMR spectra. X-ray crystal structures of HC6.Li and HC6.Cs indicate that the size of the alkali metal has some influence on the conformation of calixanions; for example, HC6.Li has a cone-like conformation, and HC6.Cs has a 1,2,3-alternate conformation. The calix[6]arene dianions show roughly the same structural architecture, and the salts tend to form polymeric chains. For most calixarene salts cation-pi arene interactions were observed.
The synthesis and full characterization (mp, NMR, UV/vis, FTIR, and elemental analysis) of 13 bismuth aryloxides are reported. We have prepared bismuth aryloxides with alkyl, aryl, and allylic substituents on the aryl rings. Eleven of these bismuth aryloxides have been characterized with single crystal X-ray diffraction methods. Bismuth-donor interactions (donor = aryl, methoxy) are observed in several cases. Three unexpected bismuth oxo aryloxides (6c, 9c, 11c) were also isolated. Complex C(77)H(102)Bi(4)Br(6)O(8) (6c) results from apparent C-H activation and Bi-C bond formation as a sideproduct in the synthesis of Bi(O-2,6-(i)Pr(2)-4-BrC(6)H(2))(3) (6). Cluster 9c has a Bi(32)O(56) core, and cluster C(90)H(90)Bi(4)Li(2)O(12) (11c) is the second lithium bismuth oxo cluster reported to date.
Copper and silver carbonyl and ethylene adducts supported by the highly fluorinated hydridotris(triazolyl)borate ligand [HB(3,5-(CF3)2Tz)3]- have been synthesized and characterized, and compared to the analogous complexes based on the hydridotris(pyrazolyl)borate ligand [HB(3,5-(CF3)2Pz)3]-. 1H and 13C NMR signals of the ethylene moiety of [HB(3,5-(CF3)2Tz)3]Cu(C2H4) and [HB(3,5-(CF3)2Tz)3]Ag(C2H4) appear at a relatively downfield position from the corresponding signals of the [HB(3,5-(CF3)2Pz)3]Cu(C2H4) and [HB(3,5-(CF3)2Pz)3]Ag(C2H4) complexes. This indicates the presence of relatively acidic metal sites in the [HB(3,5-(CF3)2Tz)3]- supported molecules. [HB(3,5-(CF3)2Tz)3]- is also a relatively weaker donor compared to the tris(pyrazolyl)borate version [HB(3,5-(CF3)2Pz)3]-. However, the CO stretching frequency values of [HB(3,5-(CF3)2Tz)3]CuCO (2138 cm(-1)) and [HB(3,5-(CF3)2Pz)3]CuCO (2137 cm(-1)) are essentially identical, and did not reflect the differences in the acidity of the metal sites. The analogous silver carbonyl adducts [HB(3,5-(CF3)2Tz)3]AgCO and [HB(3,5-(CF3)2Pz)3]AgCO also show similar nuCO values (2178 cm(-1)). These results illustrate the limitation of using the nu(CO) value of metal carbonyls as a sole indicator of the electronic structure of metal sites in some metal complexes, especially when the metal-->CO pi-back bonding is less important, and the nuCO values of two adducts are unexpectedly similar and appear at a region closer to that of the free CO (2143 cm(-1)).
Fluorinated tris(triazolyl)borate [HB(3,5-(CF(3))(2)Tz)(3)](-) (Tz = triazolyl) affords the isolation of [Na(THF)(6)]{[HB(3,5-(CF(3))(2)Tz)(3)](2)Na} with a ligand sandwiched sodium ion and a copper carbonyl complex [HB(3,5-(CF(3))(2)Tz)(3)]CuCO with a high C-O stretching frequency.
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