Department of Chemistry, Faculty of Science, Hokkaido University, North-10 West-8, Kita-ku, Sapporo 060-0810, Japan.
Inorg Chem. 2011 Sep 5;50(17):8308-17. doi: 10.1021/ic2008396. Epub 2011 Jul 29.
We describe the novel synthesis of a bis(hydrazone)iron(II) complex in protonated [Fe(Hpbph)(2)]Cl(2) (1) and deprotonated [Fe(pbph)(2)] (2) forms and several hydrogen-bonded proton-transfer (HBPT) assemblies having different dimensionalities of hydrogen-bonded network structures, Fe(Hpbph)(2)·2CH(3)OH (3), Fe(Hpbph)(2)(2)·2THF (4), and Fe(Hpbph)(2)(H(2)CA)(2)·2CH(3)CN (5) (Hpbph = 2-(diphenylphosphino)benzaldehyde-2-pyridylhydrazone), consisting of a deprotonated Fe(II)-hydrazone complex (2) as a proton acceptor (A) and chloranilic acid (H(2)CA) as a proton donor (D). The deprotonated complex 2 exhibited two-step reversible protonation reactions to form the double-protonated form 1, and the acid-dissociation constants were determined to be 7.6 and 10.3 in methanol solution. Utilizing this proton-accepting ability of 2, we succeeded in synthesizing HBPT assemblies 3, 4, and 5 from the reactions in CH(3)OH, THF, and CH(3)CN, respectively, with the same D/A ratio of H(2)CA/[Fe(pbph)(2)] = 10:1. These assemblies were found to have one-dimensional (1-D), two-dimensional (2-D), and three-dimensional (3-D) hydrogen-bonded networks with D/A ratios of 1:1, 2:1, and 3:1 for 3, 4, and 5, respectively. In 3, a 1-D hydrogen-bonded chain composed of the alternate arrangement of Fe(Hpbph)(2) and CA(2-), {···Fe(Hpbph)(2)···CA(2-)···}(∞), was surrounded by solvated methanol molecules to form isolated 1-D hydrogen-bonded chains. In the HBPT assembly 4, a 2-D hydrogen-bonded sheet was formed from two types of hydrogen-bonded chains, {···Fe(Hpbph)(2)···HCA(-)···HCA(-)···}(∞) and {···HCA(-)···HCA(-)···}(∞), and solvated THF molecules did not form any hydrogen bonds. In 5, two orthogonal hydrogen-bonded chains constructed from the neutral chloranilic acid molecules, {···CA(2-)···2(H(2)CA)···}(∞), were formed in addition to the 1-D hydrogen-bonded chain similar to that in 3, resulting in the formation of a rigid 3-D hydrogen-bonded network structure. By controlling the dimensionality of the hydrogen bond network, we found that the 2-D HBPT assembly 4 is sufficiently flexible to exhibit interesting vapochromic behavior in response to various organic vapors.
我们描述了一种双腙铁(II)配合物的新合成方法,该配合物存在于质子化[Fe(Hpbph)(2)]Cl(2)(1)和去质子化[Fe(pbph)(2)](2)形式中,以及几种具有不同维度氢键网络结构的氢键转移(HBPT)组装体中,包括Fe(Hpbph)(2)·2CH(3)OH(3)、Fe(Hpbph)(2)(2)·2THF(4)和Fe(Hpbph)(2)(H(2)CA)(2)·2CH(3)CN(5)(Hpbph=2-(二苯基膦基)苯甲醛-2-吡啶腙),它们由去质子化的 Fe(II)-腙配合物(2)作为质子受体(A)和氯代邻苯二甲酸(H(2)CA)作为质子供体(D)组成。去质子化的配合物 2 表现出两步可逆质子化反应,形成双质子化形式 1,酸离解常数在甲醇溶液中分别为 7.6 和 10.3。利用 2 的这种质子接受能力,我们成功地分别在甲醇、THF 和 CH(3)CN 中反应合成了 HBPT 组装体 3、4 和 5,其中 H(2)CA/[Fe(pbph)(2)]的 D/A 比为 10:1。发现这些组装体具有一维(1-D)、二维(2-D)和三维(3-D)氢键网络,对于 3、4 和 5,其 D/A 比分别为 1:1、2:1 和 3:1。在 3 中,由交替排列的Fe(Hpbph)(2)和 CA(2-)组成的 1-D 氢键链,{···Fe(Hpbph)(2)···CA(2-)···}(∞),被溶剂甲醇分子包围,形成孤立的 1-D 氢键链。在 HBPT 组装体 4 中,由两种氢键链组成的 2-D 氢键层,{···Fe(Hpbph)(2)···HCA(-)···HCA(-)···}(∞)和{···HCA(-)···HCA(-)···}(∞),以及未形成任何氢键的溶剂 THF 分子。在 5 中,除了类似于 3 的 1-D 氢键链之外,还形成了由中性氯代邻苯二甲酸分子构成的两个正交氢键链,{···CA(2-)···2(H(2)CA)···}(∞),导致形成刚性 3-D 氢键网络结构。通过控制氢键网络的维度,我们发现 2-D HBPT 组装体 4 具有足够的灵活性,能够对各种有机蒸气表现出有趣的颜色变化行为。