A reaction mechanism is the microscopic path by which reactants are transformed into products. Each step is an elementary reaction. In my other articles, you can also check out more blogs about 3030-47-5
Electric Literature of 3030-47-5, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.3030-47-5, Name is N1-(2-(Dimethylamino)ethyl)-N1,N2,N2-trimethylethane-1,2-diamine, molecular formula is C9H23N3. In a Article£¬once mentioned of 3030-47-5
Rational design of homo and hetero hexanuclear coordination compounds: Syntheses and magnetic properties of hexacopper and diocopper tetranickel coordination compounds and the crystal structure of a hexacopper coordination compound (see abstract)
New homo- and heterometallic hexanuclear complexes of formula {[Cu(tmen)(H2O)]2[Cu(tmen)]2[Cu2L](H2O)}(ClO4)4 ¡¤ 2 H2O [Cu6- tmen] {[Cu(pmdien)]4[Cu2L]}(ClO4)4 ¡¤ 4 H2O [Cu6-pmdien] and {[Ni(cyclam)]4[Cu2L]}(ClO4)4 ¡¤ 4 H2O [Cu2Ni4-cyclam] [H8L = tetrakis(aminomethylene)methanetetrakis(oxamic acid), tmen = N,N,N’,N’- tetramethylethylenediamine, pmdien = N,N,N’N’,N”- pentamethyldiethylenetriamine, and cyclam = 1,4,8,11- tetraazacyclotetradecane] have been synthesized. The crystal structure of [Cu6-tmen] has been determined by single-crystal X-ray diffraction. The structure consists of cationic {[Cu(tmen)(H2O)]2[Cu(tmen)]2- [Cu2L](H2O)}4+ hexanuclear units. The hexanuclear cation is made up of two symmetry-related oxamato-bridged trinuclear units connected through the central carbon atom C(6) of the L8- ligand. Variable-temperature magnetic susceptibility measurements (1,8-300 K) have been performed for these series of complexes including the dinuclear precursors of formula Na4[Cu2L] ¡¤ 10.5 H2O [Cu2-Na], (NMe4)4[Cu2L] ¡¤ 4 H2O [Cu2-NMe4] and (PPh4)4[Cu2L] ¡¤ 6 H2O [Cu2-PPh4]. The magnetic data have been interpreted. Evidence of a weak intramolecular ferromagnetic interaction between the two Cu(II) ions in [Cu2L]4- has been observed. For the hexanuclear species, the interaction through the oxamato bridge was found to be equal to -6790, -2650, and -1643 yJ (-342, -133, and -82 cm-1) for [Cu6-tmen], [Cu6-pmdien], and [Cu2Ni4-cyclam], respectively. In these complexes, the weak intramolecular ferromagnetic coupling between the two Cu(II) ions within the dinuclear synthon was masked by intermolecular interactions or local anisotropy.
A reaction mechanism is the microscopic path by which reactants are transformed into products. Each step is an elementary reaction. In my other articles, you can also check out more blogs about 3030-47-5
Reference£º
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI