English  |  正體中文  |  简体中文  |  全文筆數/總筆數 : 6507/11669
造訪人次 : 30045627      線上人數 : 571
RC Version 3.2 © Powered By DSPACE, MIT. Enhanced by NTU Library IR team.
搜尋範圍 進階搜尋

請使用永久網址來引用或連結此文件: http://ir.ncue.edu.tw/ir/handle/987654321/18944

題名: New Ag(I) Coordination Polymers of 2,6-pyridine-dicarboxamide: In Situ Ligand Formation and a Unique Secondary Building Unit
作者: Cheng, Pi-Yun;Chen, Chih-Yuan;Lee, Hon Man
貢獻者: 化學系
日期: 2009-04
上傳時間: 2014-08-14T04:29:34Z
出版者: Elsevier
摘要: 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.
關聯: Inorganica Chimica Acta, 362(6): 1840-1846
顯示於類別:[化學系] 期刊論文

文件中的檔案:

檔案 大小格式瀏覽次數
index.html0KbHTML499檢視/開啟


在NCUEIR中所有的資料項目都受到原著作權保護.

 


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