Complexation of Ag(i) cation to a series of substituted anthracenes (AN), phenanthrenes (PH), pyrenes (PY) and cyclopenta[a]phenanthrenes (CPaPH) was studied in competitive experiments by allowing PAHs to react in pairs with AgOTf. The resulting complexes were examined by electrospray mass spectrometry (ES-MS) to determine relative abundances of the corresponding monomeric and dimeric complexes...

A non-classic complexation mode was discovered upon spectroscopic, thermodynamic, crystallographic and computational studies of a β-cyclodextrin/propionic acid complex. A "fully immersed" complexation phenomenon, where both the guest's hydrophobic and polar moieties are located inside the host and are stabilized by it, was found and calculated as the most favorable configuration.

Complexation thermodynamics of UO22+ and a series N,N,N’,N’-tetraalkyl diglycolamide (TRDGA) ligands having alkyl chains –CH3 to –C6H13 were investigated in an ionic liquid (IL). The complexation constant for UO22+/DGA complex increased linearly with increasing chain length DGA from tetramethyl (logβ1 = 4.52, logβ2 8.01) tetrahexyl 5.62, 10.3). There two types species recorded the calorimetric ...

Characterization of metal complexation phenomena in seawater is a formidable challenge. Adequate characterization of inorganic complexation schemes is currently limited by a paucity of well-defined hydrolysis constant data for chemical species which are important in the weakly alkaline conditions of normal seawater. Other important problems include the neglect of equilibria involving ligands an...

In the present study, an investigation on the complex formation between mono- and divalent metal ions (Na+, K+, Li+ and Mg2+) in the form of salt with different podands using various solvents has been carried out.  Isolated complexes were characterized by different spectroscopic techniques viz. IR, NMR and elemental analysis. On the basis of ...

Divalent metal complexes of macrocyclic ligand 1,4,8,11-tetraazacyclotetradecane-1,8-bis(methylphosphonic acid)) (1,8-H4te2p, H4L) were investigated in solution and in the solid state. The majority of transition-metal ions form thermodynamically very stable complexes as a consequence of high affinity for the nitrogen atoms of the ring. On the other hand, complexes with Mn2+, Pb2+ and alkaline e...