scholarly journals Enhanced dielectricity coupled to spin-crossover in a one-dimensional polymer iron(ii) incorporating tetrathiafulvalene

2020 ◽  
Vol 11 (24) ◽  
pp. 6229-6235 ◽  
Author(s):  
Ya-Ru Qiu ◽  
Long Cui ◽  
Pei-Yu Cai ◽  
Fei Yu ◽  
Mohamedally Kurmoo ◽  
...  

A concerted bending–flattening motion of the redox-active TTF within constructed one-dimensional FeII–TTF–Schiff-base chain with bridging 4,4′-bpy enhances the dielectric constant coupled to its spin-crossover transition above room temperature.

2020 ◽  
Vol 59 (12) ◽  
pp. 8320-8333 ◽  
Author(s):  
Sophie Schönfeld ◽  
Katja Dankhoff ◽  
Dirk Baabe ◽  
Marc-Kevin Zaretzke ◽  
Martin Bröring ◽  
...  

Langmuir ◽  
2011 ◽  
Vol 27 (7) ◽  
pp. 4076-4081 ◽  
Author(s):  
Massimiliano Cavallini ◽  
Ilaria Bergenti ◽  
Silvia Milita ◽  
Jean Crispin Kengne ◽  
Denis Gentili ◽  
...  

2014 ◽  
Vol 67 (11) ◽  
pp. 1574 ◽  
Author(s):  
Darunee Sertphon ◽  
David J. Harding ◽  
Phimphaka Harding ◽  
Keith S. Murray ◽  
Boujemaa Moubaraki ◽  
...  

A new sterically bulky Schiff base ligand, N-(8-quinolyl)-5-tert-butylsalicylaldimine (Hqsal-5-tBu) has been prepared and a series of FeIII complexes, [Fe(qsal-5-tBu)2]Y (Y = Cl 1, ClO4 2, NO3 3, BF4 4) utilising this ligand are reported and fully characterised. UV-vis spectroscopic and electrochemical studies indicate that 1–4 are high spin (HS) in solution at room temperature and further suggest that the tBu group only slightly alters the electronic properties of 1–4 compared with related [Fe(qsal-5-X)2]+ systems. The structures of [Fe(qsal-5-tBu)2]Cl·4MeOH·H2O 1, [Fe(qsal-5-tBu)2]ClO4·MeOH 2, and [Fe(qsal-5-tBu)2]NO3 3 determined at 100 K reveal HS FeIII centres in all cases. Four-fold parallel aryl embraces and π–π interactions serve to link the cations forming 2D sheets mirroring the motifs found in other [Fe(qsal-5-X)2]+ complexes. Despite this the tBu group causes strong distortions at the Fe centre which as magnetic studies reveal prevent spin crossover trapping 1–4 in the HS state.


2008 ◽  
Vol 361 (12-13) ◽  
pp. 3489-3493 ◽  
Author(s):  
Atsuhiro Nabei ◽  
Takayoshi Kuroda-Sowa ◽  
Takashi Okubo ◽  
Masahiko Maekawa ◽  
Megumu Munakata

2020 ◽  
Vol 56 (72) ◽  
pp. 10469-10472 ◽  
Author(s):  
Lisa Zappe ◽  
Sophie Schönfeld ◽  
Gerald Hörner ◽  
Katrina A. Zenere ◽  
Chanel F. Leong ◽  
...  

A 1-D chain CP with both SCO and redox activity has been successfully prepared by the combination of a bis-pyridyl functionalised TTF core and a Schiff base-like N2O2 ligand.


2008 ◽  
Vol 47 (22) ◽  
pp. 10232-10245 ◽  
Author(s):  
M. Seredyuk ◽  
A. B. Gaspar ◽  
V. Ksenofontov ◽  
Y. Galyametdinov ◽  
M. Verdaguer ◽  
...  

2021 ◽  
Vol 9 ◽  
Author(s):  
Ya-Ru Qiu ◽  
Long Cui ◽  
Jing-Yuan Ge ◽  
Mohamedally Kurmoo ◽  
Guijun Ma ◽  
...  

Two polymorphic FeII coordination polymers [FeIIL (TPPE)0.5] 1) and [(FeII3L3 (TPPE)1.5)] 2), were obtained from a redox-active tetrathiafulvalene (TTF) functionalized ligand [H2L = 2,2’-(((2-(4,5-bis-(methylthio)-1,3-dithiol-2-ylidene)benzo(d) (1,3) dithiole-5,6-diyl)bis-(azanediyl))bis-(meth anylylidene)) (2E,2E')-bis(3-oxobutanoate)] and a highly luminescent connector {TPPE = 1,1,2,2-tetrakis[4-(pyridine-4-yl)phenyl]-ethene}. Complex 1 has a layered structure where the TPPE uses its four diverging pyridines from the TPPE ligand are coordinated by the trans positions to the flat TTF Schiff-base ligand, and complex 2 has an unprecedented catenation of layers within two interpenetrated frameworks. These coordination polymers reserved the redox activity of the TTF unit. Complex 1 shows gradual spin transition behavior without hysteresis. And the fluorescence intensity of TPPE in 1 changes in tandem with the spin crossover (SCO) transition indicating a possible interplay between fluorescence and SCO behavior.


RSC Advances ◽  
2014 ◽  
Vol 4 (74) ◽  
pp. 39126-39131 ◽  
Author(s):  
Meng-Ya Chen ◽  
Xuan-Rong Chen ◽  
Wei-Hua Ning ◽  
Xiao-Ming Ren

Monodisperse nanoparticles of one-dimensional Fe(II)-4-amino-1,2,4-triazole coordination polymers show hysteretic spin-crossover near room temperature.


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