A new application about (1S,2S)-Cyclohexane-1,2-diamine

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.Product Details of 21436-03-3, you can also check out more blogs about21436-03-3

The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.21436-03-3, Name is (1S,2S)-Cyclohexane-1,2-diamine, molecular formula is C6H14N2. In a Article£¬once mentioned of 21436-03-3, Product Details of 21436-03-3

Two CrIII-MnIII heterobimetallic compounds, [Mn((R,R)-5-MeOSalcy)Cr(Tp)(CN)3¡¤2CH3CN]n (1-RR) and [Mn((S,S)-5-MeOSalcy)Cr(Tp)(CN)3¡¤2CH3CN]n (1-SS) [Salcy = N,N?-(1,2-cyclohexanediylethylene)bis(salicylideneiminato) dianion], were synthesized by using the tricyanometalate building block, [(Tp)Cr(CN)3]- [Tp = tris(pyrazolyl) hydroborate] and chiral MnIII Schiff base precursors. Structural analyses and circular dichroism (CD) spectra revealed that 1-RR and 1-SS are a pair of enantiomers containing a neutral cyano-bridged zigzag chain with (-Cr-C?N-Mn-N?C-)n as the repeating unit. Magnetic studies show that antiferromagnetic couplings between CrIII and MnIII ions occur by cyanide bridges. 1-RR and 1-SS present metamagnetic, spin-canting, and antiferromagnetic order behaviors at low temperatures.

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.Product Details of 21436-03-3, you can also check out more blogs about21436-03-3

Reference£º
Chiral Catalysts,
Chiral catalysts – SlideShare