2015
DOI: 10.1002/zaac.201400464
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Cobalt(II) and Copper(II) Complexes Constructed from Bis(benzimidazole) and 2,6‐Pyridinedicarboxylate Co‐ligands: Synthesis, Crystal Structures, and Catalytic Properties

Abstract: Three metal complexes based on the flexible bis(benzimidazole) derivatives, namely [Co 2 (L1) 4 (pydc) 2 ]·2H 2 O (1), {[Cu(L1)(pydc)]·0.75H 2 O} n (2), and [Co 2 (L2) 2 (pydc) 2 ]·8H 2 O (3), [L1 = 1,2-bis(5,6-dimethylbenzimidazol-1-ylmethyl)benzene, H 2 pydc = 2,6-pyridinedicarboxylic acid, L2 = 1,4-bis(5-methylbenzimidazol-1-ylmethyl)benzene] were hydrothermally synthesized and characterized by IR spectra, elemental analysis, UV/Vis diffuse refraction spectroscopy, and X-ray single-crystal diffraction. Comp… Show more

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Cited by 31 publications
(12 citation statements)
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References 39 publications
(29 reference statements)
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“…Pyridine dicarboxylic acids which contain a pyridine ring and two carboxylate groups can form various coordinated geometries [9][10][11], and their complexes have been used as electron carriers in some model biological systems as specific molecular tools in DNA cleavage and as NO scavengers [12]. Among the isomers (viz 2,3-, 2,4-, 2,5-, 2,6-, 3,4-and 3,5-H 2 pdc), pyridine-2,6-dicarboxylic acid (2,6-H 2 pdc) has attracted much interest in the synthesis of compounds, because two carboxyl groups with a 120° angle can provide widely varying coordination modes and form both discrete and consecutive metal complexes under the appropriate conditions [13]. 2,6-H 2 pdc is a versatile N and O donor ligand, and it can form stable chelates with numerous metal ions and exhibit diverse coordination geometries, such as bidentate, tridentate, meridian or bridging [14,15].…”
Section: Introductionmentioning
confidence: 99%
“…Pyridine dicarboxylic acids which contain a pyridine ring and two carboxylate groups can form various coordinated geometries [9][10][11], and their complexes have been used as electron carriers in some model biological systems as specific molecular tools in DNA cleavage and as NO scavengers [12]. Among the isomers (viz 2,3-, 2,4-, 2,5-, 2,6-, 3,4-and 3,5-H 2 pdc), pyridine-2,6-dicarboxylic acid (2,6-H 2 pdc) has attracted much interest in the synthesis of compounds, because two carboxyl groups with a 120° angle can provide widely varying coordination modes and form both discrete and consecutive metal complexes under the appropriate conditions [13]. 2,6-H 2 pdc is a versatile N and O donor ligand, and it can form stable chelates with numerous metal ions and exhibit diverse coordination geometries, such as bidentate, tridentate, meridian or bridging [14,15].…”
Section: Introductionmentioning
confidence: 99%
“…All coordinated bonds are within normal distances. [25,26] The completely deprotonated nda 2-ligands adopt μ 2 -η 1 :η 1 -bidentate bridging through two carboxyl oxygen atoms con-necting the adjacent Co atoms along the bc direction to give rise to 1D zigzag chain with two kinds of Co1···Co1 separations of 13.3753(8) Å and 13.2148(8) Å and a Co1···Co1···Co1 angle of 100.759(3)° (Figure 1b). The difference observed in the Co1···Co1 separation by nda ligands can be attributed to slight adjustment in the coordination process between carboxylate groups and central Co atoms.…”
Section: Structure Description Of Complexmentioning
confidence: 97%
“…Overall, both complexes exhibited higher catalytic properties on the degradation of Congo red in a Fenton-like process than other reported complexes. [26,37,38] Since Co II species may play an important role in the reactions, hence, a further control experiment using equimolar CoCl 2 ·6H 2 O as used for the complexes were carried out under similar conditions. In the case, the degradation efficiency only reaches 55.5 %.…”
Section: Catalytic Propertiesmentioning
confidence: 99%
“…Pyridine-2-6-dicarboxylate (pydic 2− ) is a frequently used ligand and coordinates are usually in a deprotonated tridentate mode. The coordinates use the N donor atom and the two carboxylate O donor functions, including the possibility of bridging (Scheme 1) [1][2][3][4][5][6][7][8][9][10][11][12][13][14]. In contrast to this, the pydic ester ligands are neutral and have three options of tris-chelate O,N,O binding, which gives rise to three different isomers O carbonyl -M-O carbonyl (CC isomer), O carbonyl -M-O alkoxy (CA isomer), and O alkoxy -M-O alkoxy (AA isomer) (Scheme 1) while a bridging mode observed frequently for pydic 2− is less probable [15][16][17].…”
Section: Introductionmentioning
confidence: 99%