Cucos Paula, Sorace Lorenzo, Maxim Catalin, Shova Sergiu, Patroi Delia, Caneschi Andrea, Andruh Marius
Ilie Murgulescu-Institute of Physical Chemistry of the Romanian Academy , Splaiul Independentei no. 202, 060021 Bucharest, Romania.
Department of Chemistry "U. Schiff" and INSTM RU, University of Florence , Via della Lastruccia 3, 50019 Florence, Italy.
Inorg Chem. 2017 Oct 2;56(19):11668-11675. doi: 10.1021/acs.inorgchem.7b01640. Epub 2017 Sep 15.
The reactions of cobalt(II) perchlorate with a diazine tetratopic helicand, HL, in the presence of sodium carbonate afford two coordination polymers constructed from tetranuclear anionic helicates as building blocks: [CoLNa(HO)]·4HO (1) and [CoLNa(HO)]·2.7HO·DMF (2). The tetranuclear triple-stranded helicates, {CoL}, are connected in 1 by sodium(I) ions and in 2 by sodium(I) and cobalt(II) ions (HL results from the condensation reaction between 3-formylsalicylic acid and hydrazine). The crystal structures of the two compounds have been solved. In both compounds the anionic helicates interact with the assembling cations through the carboxylato oxygen atoms. Compound 2 features chains resulting from connecting the tetranuclear helicates through cobalt(II) ions. The analysis of the magnetic properties of compounds 1 and 2 evidenced a dominant antiferromagnetic coupling for 1, resulting in a diamagnetic ground state. In contrast, the magnetic behavior of 2 is dominated at low temperature by the Co ion which connects the antiferromagnetically coupled {Co} helical moieties. The ac magnetic measurements for 2 reveal the occurrence of slow relaxation of the magnetization that is due to the single, uncorrelated cobalt(II) ions, which are diluted in an essentially diamagnetic matrix of {Co} moieties (ΔE = 26.7 ± 0.3 cm with τ = (2.3 ± 0.2) × 10 s).
在碳酸钠存在的情况下,高氯酸钴(II)与二嗪四齿螺旋配体HL反应,得到两种以四核阴离子螺旋体为结构单元构建的配位聚合物:[CoLNa(HO)]·4HO (1) 和 [CoLNa(HO)]·2.7HO·DMF (2)。四核三链螺旋体{CoL}在1中通过钠离子连接,在2中通过钠离子和钴(II)离子连接(HL由3-甲酰基水杨酸与肼的缩合反应生成)。已解析出这两种化合物的晶体结构。在这两种化合物中,阴离子螺旋体通过羧基氧原子与组装阳离子相互作用。化合物2具有通过钴(II)离子连接四核螺旋体形成的链。对化合物1和2的磁性分析表明,1中存在占主导的反铁磁耦合,导致基态为抗磁性。相比之下,2的磁行为在低温下由连接反铁磁耦合的{Co}螺旋部分的钴离子主导。对2的交流磁性测量表明,由于单个不相关的钴(II)离子在基本上为抗磁性的{Co}部分基质中稀释,出现了磁化的缓慢弛豫(ΔE = 26.7 ± 0.3 cm,τ = (2.3 ± 0.2) × 10 s)。