Copper(II) Coordination Polymers Self-Assembled from Aminoalcohols and Pyromellitic Acid: Highly Active Precatalysts for the Mild Water-Promoted Oxidation of Alkanes

Abstract

Three novel water-soluble 2D copper(II) coordination polymers-[{Cu2(μ2-dmea)2(H2O)}2(μ4-pma)]n·4nH2O (1), [{Cu2(μ2-Hedea)2}2(μ4-pma)]n·4nH2O (2), and [{Cu(bea)(Hbea)}4(μ4-pma)]n·2nH2O (3)-were generated by an aqueous medium self-assembly method from copper(II) nitrate, pyromellitic acid (H4pma), and different aminoalcohols [N,N-dimethylethanolamine (Hdmea), N-ethyldiethanolamine (H2edea), and N-benzylethanolamine (Hbea)]. Compounds 2 and 3 represent the first coordination polymers derived from H2edea and Hbea. All the products were characterized by infrared (IR), electron paramagnetic resonance (EPR), and ultraviolet-visible light (UV-vis) spectroscopy, electrospray ionization-mass spectroscopy (ESI-MS(±)), thermogravimetric and elemental analysis, and single-crystal X-ray diffraction (XRD), which revealed that their two-dimensional (2D) metal-organic networks are composed of distinct dicopper(II) or monocopper(II) aminoalcoholate units and μ4-pyromellitate spacers. From the topological viewpoint, the underlying 2D nets of 1-3 can be classified as uninodal 4-connected layers with the sql topology. The structures of 1 and 2 are further extended by multiple intermolecular hydrogen bonds, resulting in three-dimensional (3D) hydrogen-bonded networks with rare or unique topologies. The obtained compounds also act as highly efficient precatalysts for the mild homogeneous oxidation, by aqueous H2O2 in acidic MeCN/H2O medium, of various cycloalkanes to the corresponding alcohols and ketones. Overall product yields up to 45% (based on cycloalkane) were attained and the effects of various reaction parameters were investigated, including the type of precatalyst and acid promoter, influence of water, and substrate scope. Although water usually strongly inhibits the alkane oxidations, a very pronounced promoting behavior of H2O was detected when using the precatalyst 1, resulting in a 15-fold growth of an initial reaction rate in the cyclohexane oxidation on increasing the amount of H2O from ∼4 M to 17 M in the reaction mixture, followed by a 2-fold product yield growth.

New Trends in Oxidative Functionalization of Carbon–Hydrogen Bonds: A Review

“…Polynuclear metal complexes containing voluminous organic [63,66,118,119,[129][130][131]186,[213][214][215][216][217][218][234][235][236][237][238][239][240][241] or siloxane [221][222][223][224][225][226][227][228] ligands are also very efficient in oxidations of organic compounds including saturated hydrocarbons with peroxides. For example, dinuclear copper complex 11 [221,224] and hexairon complex 15 (for the structure, see Figure 9) affording the products of cyclohexane oxidation in a very high yield of 46% (see Figure 10 [226]) can be considered as "inorganic models of methane monooxygenases."…”

“…Pombeiro, Martins, Guedes da Silva [234][235][236][237][238], Kirillov [234,235,[239][240][241], and other scientists [242] synthesized various polynuclear complexes, coordination polymers, and derived metal integrated mesoporous matrices and demonstrated high catalytic activity of these materials in oxidations with peroxides. Figures 13-15 show the examples of such catalysts.…”

Review: Recent advances of one-dimensional coordination polymers as catalysts

“…However, more efforts to systematically study the potential properties of lesser-dimensional CPs have been made recently [44][45][46][47][48][49][50] . Despite their structural simplicity compared to MOFs, one dimensional (1D) CPs in particular are generally easier to synthesize and the resulting framework can be tuned more effectively in order to generate structures with maximized application potential 51,52 .…”

Novel access to verbenone via ruthenium nanoparticles-catalyzed oxidation of α-pinene in neat water

“…Moreover, the influence of additional water in the reaction mixture (Table 2, Entries 5-7) has been studied, since some authors recently reported its promoting effect on the reaction rate in cyclohexane oxidation. [51] However, no beneficial effect of water addition has been observed in the oxidation of -pinene under optimized conditions. Moreover, the addition of a co-solvent, which could improve the solubility of the terpenic olefin, did not improve the results (Table 2, Entry 8).…”