English  |  正體中文  |  简体中文  |  Items with full text/Total items : 6498/11670
Visitors : 25658393      Online Users : 74
RC Version 3.2 © Powered By DSPACE, MIT. Enhanced by NTU Library IR team.
Scope Adv. Search

Please use this identifier to cite or link to this item: http://ir.ncue.edu.tw/ir/handle/987654321/18944

Title: New Ag(I) Coordination Polymers of 2,6-pyridine-dicarboxamide: In Situ Ligand Formation and a Unique Secondary Building Unit
Authors: Cheng, Pi-Yun;Chen, Chih-Yuan;Lee, Hon Man
Contributors: 化學系
Date: 2009-04
Issue Date: 2014-08-14T04:29:34Z
Publisher: Elsevier
Abstract: The hydrothermal reactions of 2,6-dicyanopyridine with AgX (X = NO3, ClO4, BF4) yielded intriguing network structures. The syntheses involve in situ generation of 2,6-pyridine-dicarboxamide (pcam), forming [Ag(pcam)2X]n·mH2O [X = NO3 (1), m = 0; BF4 (2), m = 1; ClO4 (3), m = 1]. These solids contain an unprecedented SBU, involving simultaneous AgO bonds/interactions and NH···O hydrogen bonding. The SBUs combine to form 2D square grids, which are stacked orderly by weak Ag···O contacts and π–π stacking interactions, forming 3D networks with infinite 1D channels, in which anions are residing. Weak Ag···O interactions play a key role in these solids and they display dynamic behaviors in solution as demonstrated by NMR spectroscopy and ESI-MS. The importance of the supramolecular synthons in the SBU was demonstrated by varying the structure of the organic tecton. Attempts to prepare similar network structures based on stronger OH···O interactions from pyridine-2,6-dicarboxylic acid (H2dipic) afforded a topologically different 2D coordination polymer.
Relation: Inorganica Chimica Acta, 362(6): 1840-1846
Appears in Collections:[化學系] 期刊論文

Files in This Item:

File SizeFormat

All items in NCUEIR are protected by copyright, with all rights reserved.


DSpace Software Copyright © 2002-2004  MIT &  Hewlett-Packard  /   Enhanced by   NTU Library IR team Copyright ©   - Feedback