Jump to main content
US EPA
United States Environmental Protection Agency
Search
Search
Main menu
Environmental Topics
Laws & Regulations
About EPA
Health & Environmental Research Online (HERO)
Contact Us
Print
Feedback
Export to File
Search:
This record has one attached file:
Add More Files
Attach File(s):
Display Name for File*:
Save
Citation
Tags
HERO ID
1526792
Reference Type
Journal Article
Title
Infinite Copper(II) Coordination Architectures from a Resonative Aminotriazine-Derived Tripodal Ligand: Synthesis, Structures, and Magnetic Properties
Author(s)
Tsai, MJ; Wu, JY; Chiang, MH; Huang, CH; Kuo, MY; Lai, LL
Year
2012
Is Peer Reviewed?
Yes
Journal
Inorganic Chemistry
ISSN:
0020-1669
EISSN:
1520-510X
Volume
51
Issue
22
Page Numbers
12360-12371
Language
English
PMID
23121020
DOI
10.1021/ic3016854
Web of Science Id
WOS:000311173700033
Abstract
The ligand 2,4,6-tris(2-picolylamino)-1,3,5-triazine (o-H(3)tpat) with essentially resonative structure and two copper(II)-based one-dimensional coordination chain structures, [Cu(3)Cl(5)(o-H(2)tpat)(H(2)O)]·MeOH·CH(2)Cl(2) (1) and [Cu(2)(o-H(2)tpat)(H(2)O)(MeOH)(NO(3))(2)](NO(3))·3MeOH (2), with different structural patterns have been synthesized and characterized using single crystal X-ray diffraction analysis. For o-H(3)tpat, two crystalline forms showing different solid-state structural features are obtained from MeOH/Et(2)O (form I) and CH(2)Cl(2)/Et(2)O (form II), respectively. The o-H(3)tpat form I adopts an asymmetric-configured all-amino resonative tautomer with three cis-trans-trans-arranged pyridyl groups, whereas the o-H(3)tpat form II adopts also an identical resonative structure but where two of the three pyridyl groups are in a cis-manner and the third one is nearly coplanar with the central aminotriazine core. On the other hand, the designed tripodal ligand in both Cu(II)-complexes serves as a monoanion, o-H(2)tpat(-), which suits a propeller-configured all-imino resonative structure in 1 and a syn-anti-configured amino-imino-imino resonative structure in 2. These observations significantly indicate that the o-H(3)tpat ligand can self-adjust and interconvert its conformation via a possible structure transformation associated with proton-shift to adapt a change in the crystallization and self-assembly reaction systems. In the magnetic point of view, 1 is treated as repeated chains composed of infinite {Cu(6)Cl(10)} units wherein the hexanuclear unit is further decomposed to one {Cu(II)(4)Cl(6)} and two magnetically isolated {Cu(II)Cl(2)} subunits. Antiferromagnetic interactions are found for the Cu(4) subunits (g = 2.33, 2J(1) = -5.6 cm(-1), 2J(2) = -8.6 cm(-1), 2J(3) = -4.1 cm(-1), and J(4) held to zero). For 2, it is considered as an infinite chain that composes of Cu(2) units antiferromagnetically coupled (g = 2.03, 2J(1) = -0.2 cm(-1)). The small antiferromagnetic exchange constants in both 1 and 2 suggest that the unpaired spins do not effectively interact through the tripodal o-H(2)tpat(-) ligands.
Tags
OPPT REs
•
OPPT_Methylene Chloride_F. Human Health
Total – title/abstract screening
Off topic
Home
Learn about HERO
Using HERO
Search HERO
Projects in HERO
Risk Assessment
Transparency & Integrity