Both spacer length and parity influence the thermal and light-induced properties of iron(II) α,ω-bis(tetrazole-1-yl)alkane coordination polymers

被引:78
作者
Absmeier, A
Bartel, M
Carbonera, C
Jameson, GNL
Weinberger, P
Caneschi, A
Mereiter, K
Létard, JF
Linert, W
机构
[1] Vienna Univ Technol, Inst Appl Synth Chem, A-1060 Vienna, Austria
[2] Univ Florence, LAMM, Dipartimento Chim, I-50019 Sesto Fiorentino, Italy
[3] Univ Florence, UdR INSTM, I-50019 Sesto Fiorentino, Italy
[4] Univ Bordeaux 1, CNRS, UPR 9048,Grp Sci Mol, Inst Chim Mat Condensee Bordeaux, F-33608 Pessac, France
[5] Vienna Univ Technol, Inst Chem Technol & Analyt, A-1060 Vienna, Austria
关键词
iron; magnetic properties; nitrogen heterocycles; organic-inorganic hybrid composites; photo-magnetism; spin crossover;
D O I
10.1002/chem.200500941
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A new series of [mu-tris-{1,n-bis(tetrazol-1-yl)alkane-N4,N4'}iron(II)] bis(perchlorate) spin-crossover coordination polymers ([Fe(nditz)(3)](ClO4)(2)]; n=4-9) has been synthesised and characterised. The ditetrazole bridging ligands provide octahedral symmetry at the iron(II) centres while allowing the distance between iron(II) centres to be varied. These polymers have therefore been investigated to determine the effects of spacer length on their thermal and light-induced spin-transition behaviour. An increase in the number of carbon atoms in the spacer (n) raises the thermal spin-crossover temperature, while decreasing the stability of the light-induced metastable state generated through the light-induced excited spin state trapping (LIESST) effect by irradiating the sample at 530 nm. Remarkably, however, the parity of the spacer also has an effect, enabling the series of complexes to be divided into two sub-series depending on whether the bridging ligand possesses an even or an odd number of carbon atoms. An explanation at the molecular level using the single configurational coordinate (SCC) model is presented.
引用
收藏
页码:2235 / 2243
页数:9
相关论文
共 33 条
[1]  
*BRUK AXS INC, 2001, XPREP VERS 5 1
[2]  
*BRUK AXS INC, 2001, SHELXTL VERS 5 1
[3]  
*BRUK AXS INC, 2001, SAINT VERS 6 2 9
[4]  
*BRUK AXS INC, 2001, PROGR SMART VERS 5 0
[5]  
Bruker AXS Inc, 2001, SADABS VERS 2 03
[6]   THERMAL AND LIGHT-INDUCED SPIN-CROSSOVER IN IRON(II) COMPLEXES WITH MONODENTATE TETRAZOLE LIGANDS CARRYING LONG ALKYL CHAINS IN THE 1-POSITION [J].
BUCHEN, T ;
GUTLICH, P .
CHEMICAL PHYSICS LETTERS, 1994, 220 (3-5) :262-266
[7]   Optically switchable behaviour of a dioxolene adduct of a cobalt-macrocycle complex [J].
Carbonera, C ;
Dei, A ;
Sangregorio, C ;
Létard, JF .
CHEMICAL PHYSICS LETTERS, 2004, 396 (1-3) :198-201
[8]   Photo-switching spin pairs-synergy between LIESST effect and magnetic interaction in an iron(II) binuclear spin-crossover compound [J].
Chastanet, G ;
Gaspar, AB ;
Real, JA ;
Létard, JF .
CHEMICAL COMMUNICATIONS, 2001, (09) :819-820
[9]   LIGHT-INDUCED EXCITED-SPIN-STATE TRAPPING IN IRON(II) SPIN-CROSSOVER SYSTEMS - OPTICAL SPECTROSCOPIC AND MAGNETIC-SUSCEPTIBILITY STUDY [J].
DECURTINS, S ;
GUTLICH, P ;
HASSELBACH, KM ;
HAUSER, A ;
SPIERING, H .
INORGANIC CHEMISTRY, 1985, 24 (14) :2174-2178
[10]   TETRAZOLES AS LIGANDS .4. IRON(II) COMPLEXES OF MONOFUNCTIONAL TETRAZOLE LIGANDS, SHOWING HIGH-SPIN REVERSIBLE LOW-SPIN TRANSITIONS [J].
FRANKE, PL ;
HAASNOOT, JG ;
ZUUR, AP .
INORGANICA CHIMICA ACTA-ARTICLES, 1982, 59 (01) :5-9