Chemical assembly of an antiferromagnetic macrocyclic molecule containing two inner CoII centers from polymeric cobalt pivalate
摘要:
The reaction of the polymer {Co(Piv)(2)}(n) (Piv is the pivalic acid anion) with triethylenetetramine (L-1) (M:L-1 = 2:1) in MeCN affords the polymeric compound [Co2L1(eta(2)-Piv)(2)(mu-Piv)(2)](n) (1) containing asymmetric dicobalt units coordinated by one chelate ligand L-1. The reaction of 1 with an additional amount of L-1 (M:L-1 = 1:1) in MeCN gives rise to the binuclear molecule Co2L21(Piv)(4) (2), where L-1 acts as a chelate-bridging ligand. Compounds analogous to 2 with M = Fe (3) were prepared by the reaction of the polymer {Fe(Piv)(2)}(n) with L-1 in MeCN using the reagent ratio M:L-1 = 1:1. The reaction of the compound CoL21(Piv)(4) (2) with isophthalaldehyde (L-2) produces the binuclear complex Co2L3(Piv)(4) (4) containing the new [2 + 2] macrocyclic ligand L-3 as a result of condensation of L-1 with L-2. All newly synthesized compounds were characterized by X-ray diffraction and magnetic measurements. (c) 2008 Elsevier Ltd. All rights reserved.
Chemical assembly of an antiferromagnetic macrocyclic molecule containing two inner CoII centers from polymeric cobalt pivalate
摘要:
The reaction of the polymer {Co(Piv)(2)}(n) (Piv is the pivalic acid anion) with triethylenetetramine (L-1) (M:L-1 = 2:1) in MeCN affords the polymeric compound [Co2L1(eta(2)-Piv)(2)(mu-Piv)(2)](n) (1) containing asymmetric dicobalt units coordinated by one chelate ligand L-1. The reaction of 1 with an additional amount of L-1 (M:L-1 = 1:1) in MeCN gives rise to the binuclear molecule Co2L21(Piv)(4) (2), where L-1 acts as a chelate-bridging ligand. Compounds analogous to 2 with M = Fe (3) were prepared by the reaction of the polymer {Fe(Piv)(2)}(n) with L-1 in MeCN using the reagent ratio M:L-1 = 1:1. The reaction of the compound CoL21(Piv)(4) (2) with isophthalaldehyde (L-2) produces the binuclear complex Co2L3(Piv)(4) (4) containing the new [2 + 2] macrocyclic ligand L-3 as a result of condensation of L-1 with L-2. All newly synthesized compounds were characterized by X-ray diffraction and magnetic measurements. (c) 2008 Elsevier Ltd. All rights reserved.