Calixarene and Resorcarene Based Receptors: From Structural and Thermodynamic Studies to the Synthesis of a New Mercury(II) Selective Material


Autoria(s): NAMOR, Angela F. Danil de; APARICIO-ARAGON, Walther; NWOGU, Nwanyinnaya; GAMOUZ, Abdelaziz El; PIRO, Oscar E.; CASTELLANO, Eduardo Ernesto
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

20/10/2012

20/10/2012

2011

Resumo

Materials used in current technological approaches for the removal of mercury lack selectivity. Given that this is one of the main features of supramolecular chemistry, receptors based on calix[4]arene and calix[4]resorcarene containing functional groups able to interact selectively with polluting ions while discriminating against biologically essential ones were designed. Thus two receptors, a partially functionalized calix[4]arene derivative, namely, 5,11,17,23-tetra-tert-butyl [25-27-bis(diethyl thiophosphate amino)dihydroxy] calix[4]arene (1) and a fully functionalized calix[4]resorcarene, 4,6,10,12,16,18,22,24-diethyl thiophosphate calix[4]resorcarene (2) are introduced. Mercury(II) was the identified target due to the environmental and health problems associated with its presence in water Thus following the synthesis and characterization of 1 and 2 in solution ((1)HNMR) and in the solid state (X-ray crystallography) the sequence of experimental events leading to cation complexation studies in acetonitrile and methanol ((1)H NMR, conductance, potentiometric, and calorimetric measurements) with the aim of assessing their behavior as mercury selective receptors are described. The cation selectivity pattern observed in acetonitrile follows the sequence Hg(II) > Cu(II) > Ag(I). In methanol 1 is also selective for Hg(II) relative to Ag(I) but no interaction takes place between this receptor and Cu(II) in this solvent. Based on previous results and experimental facts shown in this paper, it is concluded that the complexation observed with Cu(II) in acetonitrile occurs through the acetonitrile-receptor adduct rather than through the free ligand. Receptor 2 has an enhanced capacity for uptaking Hg(II) but forms metalate complexes with Cu(II). These studies in solution guided the inmobilization of receptor 1 into a silica support to produce a new and recyclable material for the removal of Hg(II) from water. An assessment on its capacity to extract this cation from water relative to Cu(II) and Ag (I) shows that the cation selectivity pattern of the inmobilized receptor is the same as that observed for the free receptor in methanol. These findings demonstrate that fundamental studies play a critical role in the selection of the receptor to be attached to silicates as well as in the reaction medium used for the synthesis of the new decontaminating agent.

European Commission[509159]

European Commission

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

FAPESP of Brazil

CONICET of Argentina

Consejo Nacional de Investigaciones Científicas y Técnicas de Argentina (CONICET)

Identificador

JOURNAL OF PHYSICAL CHEMISTRY B, v.115, n.21, p.6922-6934, 2011

1520-6106

http://producao.usp.br/handle/BDPI/29926

10.1021/jp110195f

http://dx.doi.org/10.1021/jp110195f

Idioma(s)

eng

Publicador

AMER CHEMICAL SOC

Relação

Journal of Physical Chemistry B

Direitos

restrictedAccess

Copyright AMER CHEMICAL SOC

Palavras-Chave #SOFT METAL-CATIONS #GAS-PHASE STRUCTURE #LOWER RIM #TETRAETHYL RESORCARENE #VERSATILE BEHAVIOR #ANION RECOGNITION #ESI-FTICRMS #SINGLE IONS #COMPLEXES #ACETONITRILE #Chemistry, Physical
Tipo

article

original article

publishedVersion