Guest-Induced Asymmetry in a Metal−Organic Porous Solid with Reversible Single-Crystal-to-Single-Crystal Structural Transformation

2005 ◽  
Vol 127 (49) ◽  
pp. 17152-17153 ◽  
Author(s):  
Tapas Kumar Maji ◽  
Golam Mostafa ◽  
Ryotaro Matsuda ◽  
Susumu Kitagawa
CrystEngComm ◽  
2012 ◽  
Vol 14 (12) ◽  
pp. 4153 ◽  
Author(s):  
Sudip Mohapatra ◽  
Hiroshi Sato ◽  
Ryotaro Matsuda ◽  
Susumu Kitagawa ◽  
Tapas Kumar Maji

2008 ◽  
Vol 130 (9) ◽  
pp. 2869-2876 ◽  
Author(s):  
Suzanne M. Neville ◽  
Gregory J. Halder ◽  
Karena W. Chapman ◽  
Martin B. Duriska ◽  
Peter D. Southon ◽  
...  

Polymers ◽  
2018 ◽  
Vol 10 (9) ◽  
pp. 1014 ◽  
Author(s):  
Chih-Chieh Wang ◽  
Szu-Yu Ke ◽  
Kuan-Ting Chen ◽  
Ning-Kuei Sun ◽  
Wei-Fang Liu ◽  
...  

An entangled composite compound, [Ni4(dpe)4(btc)2(Hbtc)(H2O)9]·3H2O (1), where H3btc = 1,3,5-benzenetricarboxylic acid and dpe = 1,2-bis(4-pyridyl)ethane, has been synthesized and structurally characterized. Single-crystal structural determination reveals that compound 1 consists of four coordination polymers (CPs), with two two-dimensional (2D) (4,4) layered metal-organic frameworks (MOFs) of [Ni(dpe)(Hbtc)(H2O)] and [Ni(dpe)(btc)(H2O)]− anion, and two one-dimensional (1D) polymeric chains of [Ni(dpe)(btc)(H2O)3]− anion and [Ni(dpe)(H2O)4]2+ cation, respectively. The three-dimensional (3D) supramolecular architecture of 1 is constructed via the inter-penetration of inter-digited, double-layered, 2D rectangle-grid MOFs by two 1D coordination polymeric chains, and tightly entangled together via the combination of inter-CPs π–π stacking and hydrogen bonding interactions. The ad-/de-sorption isotherms of 1 for water displays a hysteresis profile with a maximum adsorption of 17.66 water molecules of per molecule unit at relative P/P0 < 0.89. The reversible de-/re-hydration processes in 1 monitored by cyclic water de-/ad-sorption TG analysis and PXRD measurements evidence a sponge-like water de-/ad-sorption property associated with a thermal-induced solid-state structural transformation. The magnetic property of 1 suggests that the ferromagnetic coupling might refer to a stronger inter-Ni(II) interaction, which could be along the btc3− or Hbtc2− ligands; the antiferromagnetic coupling corresponding to the weaker inter-Ni(II) interactions, which could be the dpe ligands for the 2D framework.


Crystals ◽  
2019 ◽  
Vol 9 (1) ◽  
pp. 45 ◽  
Author(s):  
Aleksandra Pacanowska ◽  
Mateusz Reczyński ◽  
Beata Nowicka

The 1D {[CuII(cyclam)]3[WV(CN)8]2.5H2O}n (1·5H2O) (cyclam = 1,4,8,11-tetraazacyclotetradecane) coordination polymer of ladder topology can be obtained in water-alcohol solution from [Cu(cyclam)]2+ and [W(CN)8]3− building blocks. Upon dehydration, 1·5H2O undergoes a single-crystal-to-single-crystal structural transformation to the anhydrous {[CuII(cyclam)]3[WV(CN)8]2}n (1) form, which retains the same topology, but is characterized by shorter Cu-W distances and significantly more bent CN-bridges. The deformation of the coordination skeleton is reflected in magnetic properties: the predominant intra-chain interactions change from ferromagnetic in 1·5H2O to antiferromagnetic in 1. The reaction between the same building blocks in water solution under slow diffusion conditions leads to the formation of a 0D {[CuII(cyclam)(H2O)]2[CuII(cyclam)][WV(CN)8]2}.3H2O pentanuclear assembly (2·3H2O).


2015 ◽  
Vol 51 (15) ◽  
pp. 3173-3176 ◽  
Author(s):  
Susan Sen ◽  
Subhadip Neogi ◽  
Kari Rissanen ◽  
Parimal K. Bharadwaj

Guest solvent triggered reversible structural transformation and concomitant Zn(ii) to Cu(ii) transmetalation has been realized through single-crystal to single-crystal fashion in an imidazolium functionalized 3D cationic Zn(ii)-framework.


2015 ◽  
Vol 21 (12) ◽  
pp. 4703-4711 ◽  
Author(s):  
Quan-Quan Li ◽  
Chun-Yan Ren ◽  
Yang-Yang Huang ◽  
Jian-Li Li ◽  
Ping Liu ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document