10.1021/cg800827a.s002
Chih-Chieh Wang
Chih-Chieh
Wang
Meu-Ju Ke
Meu-Ju
Ke
Cheng-Hsiao Tsai
Cheng-Hsiao
Tsai
I-Hsuan Chen
I-Hsuan
Chen
Shin-I Lin
Shin-I
Lin
Tzuen-Yeuan Lin
Tzuen-Yeuan
Lin
Li-Mei Wu
Li-Mei
Wu
Gene-Hsiang Lee
Gene-Hsiang
Lee
Hwo-Shuenn Sheu
Hwo-Shuenn
Sheu
Vladimir E. Fedorov
Vladimir E.
Fedorov
[M(C<sub>5</sub>O<sub>5</sub>)<sub>2</sub>(H<sub>2</sub>O)<sub><i>n</i></sub>]<sup>2−</sup> as a Building Block for Hetero- and Homo-bimetallic Coordination Polymers: From 1D Chains to 3D Supramolecular Architectures
American Chemical Society
2009
coordination modes
dimeric structure
croconate bridge
C 5O
3 D Supramolecular ArchitecturesA series
water molecules
croconate acts
bidentate
1 D Chains
Structural determination
supramolecular architectures
coordination polymers
Cu
dianion
building block
Building Block
hydrogen bonds
2009-02-04 00:00:00
Dataset
https://acs.figshare.com/articles/dataset/_M_C_sub_5_sub_O_sub_5_sub_sub_2_sub_H_sub_2_sub_O_sub_i_n_i_sub_sup_2_sup_as_a_Building_Block_for_Hetero_and_Homo_bimetallic_Coordination_Polymers_From_1D_Chains_to_3D_Supramolecular_Architectures/2881138
A series of one-dimensional (1D) coordination polymers, {[Cu(en)<sub>2</sub>][M(C<sub>5</sub>O<sub>5</sub>)<sub>2</sub>(H<sub>2</sub>O)<sub><i>m</i></sub>]·<i>x</i>H<sub>2</sub>O}<i><sub>n</sub></i>, (M = Mn (<b>1</b>), <i>m</i> = 4, <i>x</i> = 2; M = Co (<b>2</b>), Ni (<b>3</b>), Cu (<b>4</b>), Zn (<b>5</b>), <i>m</i> = 2, <i>x</i> = 0; en = ethylenediamine; C<sub>5</sub>O<sub>5</sub><sup>2−</sup> = croconate, dianion of 4,5-dihydroxycyclopent-4-ene-1,2,3-trione), using [M(C<sub>5</sub>O<sub>5</sub>)<sub>2</sub>(H<sub>2</sub>O)<i><sub>n</sub></i>]<sup>2−</sup> dianion as a building block has been synthesized and characterized by the X-ray diffraction method. Structural determination reveals that, in compounds <b>1</b>−<b>5</b>, one [M(C<sub>5</sub>O<sub>5</sub>)<sub>2</sub>(H<sub>2</sub>O)<sub><i>n</i></sub>]<sup>2−</sup> dianion coordinates via two oxygen (croconate) donors to the axial sites of two Cu(II) centers of [Cu(en)<sub>2</sub>]<sup>2+</sup> cations to form one-dimensional (1D) linear (<b>1</b>, <b>3</b> and <b>4</b>) or zigzag (<b>2</b> and <b>5</b>) chains of alternating [M(C<sub>5</sub>O<sub>5</sub>)<sub>2</sub>(H<sub>2</sub>O)<sub><i>n</i></sub>]<sup>2−</sup> and [Cu(en)<sub>2</sub>]<sup>2+</sup> units. The croconate acts as a bridging ligand with three coordination modes as μ<sub>1,3</sub>-bismonodentate for <b>1</b>, μ<sub>1,2,3</sub>-bidentate/monodentate for <b>2</b> and <b>5</b>, and μ<sub>1,2,4</sub>-bidentate/monodentate for <b>3</b> and <b>4</b>, respectively. In addition, a byproduct, [Cu(en)(C<sub>5</sub>O<sub>5</sub>)(H<sub>2</sub>O)]<sub>2</sub> (<b>6</b>), which is cocrystallized with <b>4</b>, shows a dimeric structure formed through the croconate bridge with μ<sub>1,1,2</sub>-bidentate/monodentate coordination mode. All of their 1D frameworks (<b>1</b>−<b>5</b>) and dimeric structure (<b>6</b>) are extended to three-dimensional (3D) supramolecular architectures by the intermolecular π−π interaction among croconates and intermolecular hydrogen bonds among the en, croconate, and coordinated water molecules.