category: Tetrahydropyrans, Because a catalyst decreases the height of the energy barrier, its presence increases the reaction rates of both the forward and the reverse reactions by the same amount. 499-40-1, Name is (2R,3S,4R,5R)-2,3,4,5-Tetrahydroxy-6-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)hexanal, molecular formula is C12H22O11. In a patent, introducing its new discovery.
Six new structures of Cd(II) complexes containing Hdpa ligands have been determined. With chloride and bromide, Cd(II) ions produce halide-bridged dinuclear units 1 and 2 while CdI2 produces mononuclear unit 3 without halide-bridging. Cd(II) ions produce mono-Hdpa complex 4 with chelating benzoate, di-Hdpa complex 5 with coordinating NO3- anion, and tri-Hdpa complexes 6 and 7 with non-coordinating ClO4- and BF4- anions. One-, two-, or three-dimensional structures of Cd(II)-Hdpa complexes can be produced by hydrogen bonding interactions and pi-pi interactions. The compounds 4, 5, and 6 catalyzed efficiently the transesterification of a variety of esters with methanol, while 1, 2, 3 and 7 have displayed a very slow conversion. The transesterification reactivity shown by the catalyst 6 is very efficient and the best among the compounds 1-7. In addition, all compounds 1-7 and ligand (Hdpa) have shown the similar luminescent properties at lambdamax = 352 nm which suggest that their emissions seem to be attributed to the pi-pi* intraligand fluorescence.
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Reference：
Tetrahydropyran – Wikipedia,
Tetrahydropyran – an overview | ScienceDirect Topics