Mareque-Rivas Juan C, Prabaharan Ravi, Parsons Simon
School of Chemistry, The University of Edinburgh, Joseph Black Building, King's Buildings, West Mains Road, Edinburgh, UK EH9 3JJ.
Dalton Trans. 2004 May 21(10):1648-55. doi: 10.1039/b402084g. Epub 2004 Apr 14.
Ligands derived from the tripodal N4 ligand tris(pyridylmethyl)amine ((pyCH2)3N, tpa) of general formula (6-RNHpyCH2)nN(CH2py)(3-n)(R = H, n= 1-3 L(1-3); R = neopentyl, n= 1-3 L'(1-3)) were used to elucidate and quantify the magnitude of the effects exerted by hydrogen bonding and hydrophobic environments in the zinc-water acidity of their complexes. The pKa of the zinc-bound water molecule of [(L(1-3))Zn(OH2)]2+ and [(L'(1-3))Zn(OH2)]2+ 1'-3' was determined by potentiometric pH titrations in water (1-3) or water-ethanol (1:1) (1'-3'). The zinc(II) water acidity gradually increases as the number of -NH2 hydrogen bonding groups adjacent to the water molecule increases. Thus, the zinc-bound water of [(L3)Zn(OH2)]2+ and [(tpa)Zn(OH2)]2+ deprotonate with pKa values of 6.0 and 8.0, respectively. The pKa of the water molecule, however, is only raised from 8.0 in [(tpa)Zn(OH2)]2+ to 9.1 in [(bpg)Zn(OH2)]+ (bpa =(pyCH2)2N(CH2COO-)). Moreover, the acidity of the zinc-bound water of several of the five-coordinate zinc(II) complexes with the hydrogen bonding groups is greater than that of four-coordinate [((12)aneN3)Zn(OH2)]2+ (pKa = 7.0). This result shows that the magnitude of the effect exerted by the hydrogen bonding groups can be larger than that induced by changing one neutral by one anionic ligand, and/or even by changing the coordination number of the zinc(II) centre. The X-ray structure of [(L'2)Zn(OH)]ClO4 2' and [(L'3)Zn(OH)]ClO4.CH3CN 3'.CH3CN is reported, and show the neopentylamino groups forming N-H...O hydrogen bonds with the zinc-bound hydroxide. Although, which have hydrogen bonding and hydrophobic groups, have a zinc-bound water more acidic than [(tpa)Zn(OH2)]2+, their pKa is not always lower than that of 1-3. This result suggests that a hydrogen bonding microenvironment may be more effective than a hydrophobic one to increase the zinc-water acidity.
源自通式为(6-RNHpyCH2)nN(CH2py)(3-n)(R = H,n = 1 - 3,L(1 - 3);R = 新戊基,n = 1 - 3,L'(1 - 3))的三脚架型N4配体三(吡啶甲基)胺((pyCH2)3N,tpa)的配体,被用于阐明和量化氢键和疏水环境对其配合物中锌-水酸度所产生影响的大小。通过在水(1 - 3)或水-乙醇(1:1) (1'-3')中进行电位pH滴定,测定了[(L(1 - 3))Zn(OH2)]2+和[(L'(1 - 3))Zn(OH2)]2+ 1'-3'中与锌结合的水分子的pKa。随着与水分子相邻的-NH2氢键基团数量增加,锌(II)水的酸度逐渐增大。因此,[(L3)Zn(OH2)]2+和[(tpa)Zn(OH2)]2+中与锌结合的水分别以pKa值6.0和8.0去质子化。然而,水分子的pKa仅从[(tpa)Zn(OH2)]2+中的8.0升高到[(bpg)Zn(OH2)]+(bpa =(pyCH2)2N(CH2COO-))中的9.1。此外,几种带有氢键基团的五配位锌(II)配合物中与锌结合的水的酸度大于四配位的[((12)aneN3)Zn(OH2)]2+(pKa = 7.0)。这一结果表明,氢键基团所产生影响的大小可能大于由一个中性配体换成一个阴离子配体,和/或甚至由改变锌(II)中心的配位数所引起的影响。报道了[(L'2)Zn(OH)]ClO4 2'和[(L'3)Zn(OH)]ClO4.CH3CN 3'.CH3CN的X射线结构,显示新戊基氨基基团与与锌结合的氢氧化物形成N-H...O氢键。尽管它们具有氢键和疏水基团,其与锌结合的水比[(tpa)Zn(OH2)]2+更酸,但其pKa并不总是低于1 - 3中的pKa。这一结果表明,氢键微环境在增加锌-水酸度方面可能比疏水微环境更有效。