Literature DB >> 17013966

A new macrocyclic cryptand with squaramide moieties: an overstructured Cu(II) complex that selectively binds halides: synthesis, acid/base- and ligational behavior, and crystal structures.

Gianluca Ambrosi1, Mauro Formica, Vieri Fusi, Luca Giorgi, Annalisa Guerri, Mauro Micheloni, Paola Paoli, Roberto Pontellini, Patrizia Rossi.   

Abstract

The synthesis and characterization of the novel 24,29-dimethyl-6,7,15,16-tetraoxotetracyclo-[19.5.5.0(5,8).0(14,17)]-1,4,9,13,18,21,24,29-octaazaenatriaconta-Delta(5,8),Delta(14,17)-diene (L) are reported. Molecule L incorporates two squaramide functions in a overstructured chain connecting two opposite nitrogen atoms of the Me(2)[12]aneN(4) polyaza macrocyclic base to obtain a cage topology. The basicity and binding properties of L towards Cu(II) were determined by means of potentiometric measurements in aqueous solution (298.1+/-0.1 K, I=0.15 mol dm(-3)). Molecule L behaves as a diprotic base under the experimental conditions employed and forms only mononuclear Cu(II) complexes in which the squaramide moieties are not involved in the stabilization of the metal ion that is stabilized by the amine functions of the polyaza base inside the three-dimensional cavity. The [CuL](2+) species was tested as a host for the series of halide anions. UV-visible spectrophotometric experiments permitted the determination of the addition constants of halides to the Cu(II)-complexed species. The [CuL](2+) species binds the anions F(-), Cl(-), and Br(-) by forming the [CuLX](+) species, but does not bind the biggest I(-) anion. A trend of selectivity as a function of the hydrogen-bonding capability as well as the dimensions of the anion were established; the maximum value of selectivity was for addition of the F(-) anion (log K=4.8). This selectivity is due to the presence of the overstructured chain containing the squaramide groups up to the Me(2)[12]aneN(4) macrocyclic base. The squaramide groups, by providing hydrogen-bond contacts, permit the [CuL](2+) species to selectively bind these anions through the formation of a hydrogen-bond network with F(-) and Cl(-). The crystal structures of the [CuLF](+) and [CuLCl](+) cations support the results obtained in aqueous solution.

Entities:  

Year:  2007        PMID: 17013966     DOI: 10.1002/chem.200600793

Source DB:  PubMed          Journal:  Chemistry        ISSN: 0947-6539            Impact factor:   5.236


  2 in total

1.  The Effect of Substitution Pattern on Binding Ability in Regioisomeric Ion Pair Receptors Based on an Aminobenzoic Platform.

Authors:  Damian Jagleniec; Krzysztof Ziach; Kajetan Dąbrowa; Jan Romański
Journal:  Molecules       Date:  2019-08-18       Impact factor: 4.411

2.  Novel fluorescent probes for the fluoride anion based on hydroxy-substituted perylene tetra-(alkoxycarbonyl) derivatives.

Authors:  Fengxia Zhang; Yunlong Zhao; Yanhui Chi; Yongshan Ma; Tianyi Jiang; Xiaofeng Wei; Qian Zhao; Zhiqiang Shi; Jingmin Shi
Journal:  RSC Adv       Date:  2018-04-16       Impact factor: 3.361

  2 in total

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