6957-22-8Relevant articles and documents
Selective and reversible adsorption of cationic dyes by mixed ligand Zn(II) coordination polymers synthesized by reactant ratio modulation
Rachuri, Yadagiri,Subhagan, Sreevalsa,Parmar, Bhavesh,Bisht, Kamal Kumar,Suresh, Eringathodi
, p. 898 - 908 (2017)
Dye capture and separation through coordination polymers (CPs) has been a promising research field in recent times due to the toxic and nondegradable nature of organic dyes released into the environment from various industries as well as the reusability of CPs for the said purpose. Here, we report the synthesis and characterization of two mixed ligand CPs {[Zn2(HBTC)2(L)(H2O)2](C2H5OH)3}n (CP1) and {[Zn5(BTC)2(L)3(OH)4(H2O)2](H2O)4(CH3OH)11}n (CP2) (where H3BTC = 1,3,5-benzene tricarboxylic acid and L = 1,4-bis(4-pyridyl)-2,3-diaza-1,3-butadiene) by the stoichiometric variation of the precursors. The crystal structure analysis revealed that CP1 is a 2D network composed of a [Zn2(HBTC)2(H2O)2]n motif linked via terminal nitrogen atoms of L and CP2 is a 3D framework in which symmetrically disposed two-dimensional {[Zn5(BTC)2(L)3(OH)4(H2O)2]}n sheets composed of pentanuclear [Zn5(RCO2)6(μ3-OH)2(μ2-OH)2(H2O)2] SBUs are pillared by L ligands. Adsorption and separation of cationic dyes by CP1 and the solid-state fluorescence properties of both CPs have been investigated. Cationic dyes (RhB, MB, and MV) can be effectively adsorbed by CP1 from their aqueous solution (61%, 90%, and 97%, respectively) while the anionic dye methyl orange (MO) remains uncaptured. Dye desorption studies and CP1 as a column chromatographic filler for the separation of cationic dyes in water have also been demonstrated.
A Water-Stable Twofold Interpenetrating Microporous MOF for Selective CO2 Adsorption and Separation
Pal, Arun,Chand, Santanu,Das, Madhab C.
, p. 13991 - 13997 (2017)
Self-assembly of bent dicarboxylate linker 4,4′-sulfonyldibenzoic acid (H2SDB) and flexible N,N-donor spacer 1,4-bis(4-pyridyl)-2,3-diaza-1,3-butadiene (L) with Co(NO3)2·6H2O forms a twofold interpenetrated {[Co2(SDB)2(L)]·(H2O)4·(DMF)}n, (IITKGP-6) network via solvothermal synthesis with SQL(2,6L1) topology, which is characterized by Fourier transform infrared spectroscopy, thermogravimetric analysis, elemental analysis, powder X-ray diffraction (XRD), and single-crystal XRD. The framework is microporous with a solvent-accessible volume of 25.5% and forms a one-dimensional channel along [1-1 0] direction with the dimensions of -3.4 × 5.0 ?2. As the stability of metal-organic frameworks (MOFs) in the presence of water is a topic of significant importance while considering them for practical applications, this framework reveals its high stability toward water. The desolvated framework shows modest uptake of CO2 (50.6 and 37.4 cm3 g-1 at 273 and 295 K under 1 bar pressure, respectively), with high selectivity over N2 and CH4. Ideal adsorbed solution theory calculations show that the selectivity values of CO2/N2 (15:85) are 51.3 at 273 K and 42.8 at 295 K, whereas CO2/CH4 (50:50) selectivity values are 36 at 273 K and 5.1 at 295 K under 100 kPa. The high CO2 separation selectivity over N2 and CH4 along with its water stability makes this MOF a potential candidate for CO2 separation from flue gas mixture and landfill gas mixture as well.
Spontaneous resolution to absolute chiral induction: Pseudo-kagomé type homochiral Zn(II)/Co(II) coordination polymers with achiral precursors
Bisht, Kamal Kumar,Suresh, Eringathodi
, p. 15690 - 15693 (2013)
It is observed that conglomerate crystallization of achiral precursors yielding racemate metal organic frameworks/coordination polymers (MOFs/CPs) can be driven to absolute homochiral crystallization of the desired enantiomorph by utilizing a suitable chiral induction agent. In a series of crystallization experiments isostructural Zn and Co homochiral CPs (1P, 1M and 2P, 2M) are prepared using the achiral precursors. In the presence of enantiopure camphoric acid, the crystallization process prefers absolute chiral induction over conglomerate formation which is established by single crystal X-ray diffraction and CD spectroscopy.
A new pillared Cd-organic framework as adsorbent of organic dyes and as precursor of CdO nanoparticles
Ghomshehzadeh, Samira Gholamali,Nobakht, Valiollah,Pourreza, Nahid,Mercandelli, Pierluigi,Carlucci, Lucia
, (2020)
A new neutral cadmium-organic framework with a pillared layer structure, [Cd3(BTC)2(4-bpdb)2] (H3BTC = benzene-1,3,5-tricarboxylic acid; 4-bpdb = 1,4-bis(4-pyridyl)-2,3-diaza-1,3-butadiene), has been synthesized via solvothermal reaction of cadmium nitrate with the tricarboxylic acid H3BTC and the linear bispyridyl linker 4-bpdb. The complex has been characterized by single crystal X-ray diffraction, showing to possess a 3D porous network of jcr7 topology. The capability of the prepared MOF in adsorbing the organic dyes Congo Red (CR) and Neutral Red (NR), together with kinetics and thermodynamics of their adsorption, have been investigated in detail. The adsorption process was well described by pseudo-first order and pseudo-second order kinetics for CR and NR, respectively. In addition, conversion of the MOF 3D architecture into nano-sized cadmium oxide particles has also been studied.
Construction of five dicyanamide based coordination polymers with diverse dimensionality: Synthesis, characterization and photoluminescence study
Das, Anamika,Bhattacharya, Biswajit,Maity, Dilip Kumar,Halder, Arijit,Ghoshal, Debajyoti
, p. 585 - 591 (2016)
A family of dicyanamide bridged compounds namely {[Co(dca)4(2-abim)2]}n(1), {[Ni(dca)4(2-abim)2]}n(2), {[Cd(dca)4(2-abim)2]}n(3), {[Zn(N(CN)2)2(4-bpdb)]}n(4) and {[Cd(N(CN)2)2(4-bpdb)]}n(5); [where dca?=?dicyanamide, 2-abim?=?2-aminobenzimidazole and 4-bpdb?=?1,4-bis-(4-pyridyl)-2,3-diaza-1,3-butadiene] have been synthesized by stirring at room temperature. These compounds have been characterized by single crystal diffraction analysis, infrared spectroscopy (IR) and powder X-ray diffraction (PXRD). Complexes 1–3 are isostructural and exhibit two-dimensional (2D) metal-dca sheet with pendant 2-abim ligand. Compound 4 forms [Zn(N(CN)2)]nchains with a pendent dca and a bridging dca linker, which are further connected by bridging 4-bpdb ligands extending into a 2D layer structure. In case of compound 5 each Cd(II) centers connect with four bridging dca linkers to form [Cd(N(CN)2)]ndouble chains, which are further connected by bridging 4-bpdb ligands extending into a 2D layer structure. Here [Cd2(N(CN)2)] and 4-bpdb spacer are interpenetrated to each other and resemble polyrotaxane-type structures. Photoluminescent properties of compounds 3–5 were also studied and they exhibit nice ligands based photoluminescence properties at room temperature.
Design, synthesis and biological evaluation of Schiff’s base derivatives as multifunctional agents for the treatment of Alzheimer’s disease
Shi, Jian,Zhou, Yi,Wang, Keren,Ma, Qinge,Wei, Rongrui,Li, Qingfeng,Zhao, Yiyang,Qiao, Zhanpin,Liu, Shuang,Leng, Yumin,Liu, Wenmin,Sang, Zhipei
, p. 624 - 634 (2020/11/30)
A series of Schiff’s base derivatives was rationally designed, synthesized, and evaluated as multi-function agents for the treatment of Alzheimer’s disease (AD). The results revealed that compound 3b was a novel multifunctional agent. It acted as a highly selective monoamine oxidase-B inhibitor (IC50 = 8.4 nM), which was explained by the docking study. Compound 3b also was an antioxidant agent (2.3 eq) and could significantly inhibit self-induced Aβ1-42 aggregation (31.8%). Meanwhile, compound 3b was a selective metal chelator and could inhibit Cu2+-induced Aβ1-42 aggregation (62.3%). Furthermore, compound 3b presented good neuroprotective effects on H2O2-induced PC12 cell injury. More importantly, compound demonstrated good blood brain barrier permeability and druglike properties. Therefore, compound 3b, a promising multi-targeted active molecule, offers an attractive starting point for further study in the drug-discovery process against AD.[Figure not available: see fulltext.].
