99868-22-1Relevant academic research and scientific papers
Synthesis, characterisation and ion-binding properties of oxathiacrown ethers appended to [Ru(bpy)2]2+. Selectivity towards Hg2+, Cd2+ and Pb2+
Odhiambo, Ruth A.,Aluoch, Austin O.,Njenga, Lydia W.,Kagwanja, Stanley M.,Wandiga, Shem O.,Wendt, Ola F.
, p. 3663 - 3672 (2018/02/07)
A series of complexes with oxathiacrown ethers appended to a [Ru(bpy)2]2+ moiety have been synthesized and characterised using 1H NMR, 13C NMR, IR, electronic absorption and emission spectroscopies, mass spectrometry and elemental analyses. The complexes exhibit strong MLCT luminescence bands in the range 608-611 nm and one reversible metal centred oxidation potential in the range 1.00-1.02 V. Their selectivity and sensitivity towards Hg2+, Cd2+ and Pb2+ metal ions have been investigated using electronic absorption, luminescence, cyclic and differential pulse voltammetry titrations. Their responses towards selected cations and anions have also been investigated using electronic absorption and luminescence. While the complexes are selective towards Hg2+ and Cd2+ ions, none of them is selective towards Pb2+ ions. In particular, complex 2 gives a selective change in the UV/Vis absorbance with Hg2+ making it possible to detect mercury down to a detection limit of 68 ppm. The binding constants and limits of detection of the complexes have been calculated, with values ranging from 4.37 to 5.38 and 1.4 × 10-3 to 6.8 × 10-5 for log Ks and LOD respectively.
Substituted diether diols by ring-opening of carbocyclic and stannylene acetals
Martinez-Bernhardt, Rolando,Castro, Peter P.,Godjoian, Gayane,Gutierrez, Carlos G.
, p. 8919 - 8932 (2007/10/03)
Reduction of malonaldehyde bis(ethylene and propylene acetals) with borane or monochloroborane produces diether diols 1 and 2 in high yield. Similar reduction of glyoxal his(ethylene acetals) has only limited utility for the preparation of tetrasubstituted triethylene glycols 3. Organotin chemistry is complementary: stannylene acetals prepared from disubstituted vicinal diols can be alkylated with half an equivalent of 1,2-dibromoethane to produce tetrasubstituted triethylene glycols 3, or with two equivalents of 2-chloroethanol to produce disubstituted triethylene glycols 4.
