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Supramolecular Organisation of Polymeric Coordination Chains into a Three‐Dimensional Network with Nanosized Channels that Clathrate Large Organic Molecules
Author(s) -
Zhang XianMing,
Tong MingLiang,
Gong MengLian,
Chen XiaoMing
Publication year - 2003
Publication title -
european journal of inorganic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.667
H-Index - 136
eISSN - 1099-0682
pISSN - 1434-1948
DOI - 10.1002/ejic.200390014
Subject(s) - chemistry , monoclinic crystal system , terephthalic acid , supramolecular chemistry , crystallography , coordination polymer , molecule , ligand (biochemistry) , 4,4' bipyridine , hydrogen bond , crystal structure , bipyridine , metal organic framework , hydrothermal reaction , single crystal , hydrothermal circulation , organic chemistry , chemical engineering , polyester , biochemistry , receptor , adsorption , engineering
Hydrothermal treatment of a mixture of [Zn(MeCO 2 ) 2 ]·H 2 O, terephthalic acid, and 2,2′‐bipyridine resulted in a coordination polymer [Zn(bpy)(tp)](bpy) ( 1 ; bpy = 2,2′‐bipyridine, H 2 tp = terephthalic acid) which crystallizes in the monoclinic space group C 2/ c , M r = 541.85, a = 15.388(11), b = 21.963(11), c = 7.670(8) Å, β = 112.82(2)°, V = 2387(3) Å 3 , Z = 4, D c = 1.506 g·cm −3 . An X‐ray single‐crystal structural analysis reveals that 1 is a three‐dimensional network with nanosized channels constructed from one‐dimensional coordination chains via C−H ··· O hydrogen bonds and aromatic intercalations. TGA and XRPD showed that the porous network of 1 is very stable while the guest 2,2′‐bipyridine molecules in the channels are removable. Compound 1 shows a strong ligand‐centred emission at room temperature in the solid state. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003)
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