Alkali Metal Directed Assembly of Heterometallic Vv/M (M = Na, K, Cs) Coordination Polymers: Structures, Topological Analysis, and Oxidation Catalytic Properties

2013 ◽  
Vol 52 (15) ◽  
pp. 8601-8611 ◽  
Author(s):  
Samik Gupta ◽  
Marina V. Kirillova ◽  
M. Fátima C. Guedes da Silva ◽  
Armando J. L. Pombeiro ◽  
Alexander M. Kirillov
ChemInform ◽  
2010 ◽  
Vol 23 (5) ◽  
pp. no-no
Author(s):  
T. BAIRD ◽  
A. BENDADA ◽  
G. WEBB ◽  
J. M. WINFIELD

2018 ◽  
Vol 233 (1) ◽  
pp. 51-59
Author(s):  
Lina Zhang ◽  
Peigao Duan ◽  
Yang Liu ◽  
Jingxian Sun ◽  
Dan Zhao ◽  
...  

AbstractFour new Ln(III)-based coordination polymers (CPs), [Eu(HL)Cl2(DMF)2]·(H2L) (1), [Dy(HL)Cl2(DMF)2]·(H2L) (2), [Er(HL)Cl2(DMF)(CH3OH)]·(DMF) (3) and [Yb(HL)Cl2(DMF)(H2O)]·(DMF) (4) (H2L=2,6-bis[(3-methoxysalicylidene)hydrazinocarbonyl]pyridine) have been synthesized through the reaction of Ln(III) chloride and H2L by using the vapour diffusion method. Interestingly, Cl−as a template agent plays a vital role in the formation of the target complexes. Single-crystal X-ray diffraction studies indicate that1and2are isostructural and crystallize in triclinic space groupP1̅, while complexes3and4are isostructural and crystallize in monoclinic space groupC2/c. Variable temperature magnetization measurement (χMT–T) demonstrates possible antiferromagnetic interactions in complex2. Alternating-current (ac) susceptibility measurement furthermore indicated frequency dependence for both the in-phase (χ′) and out-of-phase (χ″) components in2, suggesting that there is a slow relaxation behavior of the magnetization, which is typical of single-molecule magnets (SMMs). This is the first time that Ln(III) CPs based on such a dihydrazone ligand has been reported so far.


2005 ◽  
Vol 277-279 ◽  
pp. 708-719
Author(s):  
Chang Seop Lee ◽  
Hee Jung Lee ◽  
Sung Woo Choi ◽  
Jahun Kwak ◽  
Charles H.F. Peden

A series of cation exchanged Y-zeolites were prepared by exchanging cations with various alkali (M+, M= Li, Na, K, Cs) metals. The structural and catalytic properties of the alkali metal exchanged Y-zeolites have been investigated by a number of analytical techniques. Comparative elemental analyses were determined by an Energy Dispersive Spectroscopy X-ray (EDS), X-ray Photoelectron Spectroscopy (XPS), Inductively Coupled Plasma-Atomic Emission Spectroscopy (ICP-AES) and X-ray Fluorescence (XRF) before and after cation substitution. The framework and non-framework Al coordination and the Si/Al ratios of the Y-zeolites were investigated by MAS Solid-State Nuclear Magnetic Resonance (NMR) spectroscopy. The Al NMR spectra were characterized by two 27Al resonance signals at 12 and 59 ppm, indicating the presence of the non-framework and framework Al respectively. The intensities of these resonances were used to monitor the amount of the framework and non-framework Al species in the series of exchanged zeolites. The 29Si NMR spectra were characterized by four resonance signals at -79, -84, -90, and -95 ppm. Changing the alkali metal cations in the exchanged Y-zeolites significantly altered the extent of the octahedral/tetrahedral coordination and the Si/Al ratio. The Fourier Transform Infrared spectra of the CO2 adsorbed on to the exchanged Y-zeolites showed a low frequency shift, as the atomic number of the exchanged alkali metal increased. In addition, the catalytic activity of these samples for NOx reduction were tested in combination with a non-thermal plasma technique and interpreted based on the above structural and spectroscopic information.


2019 ◽  
Vol 222 ◽  
pp. 81-86 ◽  
Author(s):  
Haruna Abdullahi ◽  
Ka-Lun Wong ◽  
Gin Keat Lim ◽  
Hussein Awala ◽  
Aurélie Vicente ◽  
...  

CrystEngComm ◽  
2013 ◽  
Vol 15 (42) ◽  
pp. 8483 ◽  
Author(s):  
Fangfang Zhao ◽  
Guangju Zhang ◽  
Huan Dong ◽  
Wenbin Ji ◽  
Lei Zhou ◽  
...  

1991 ◽  
Vol 68 (1) ◽  
pp. 31-39 ◽  
Author(s):  
C.P. Nicolaides ◽  
M. Wapiennik ◽  
K.I.G. Weiss ◽  
H. van den Akker ◽  
B. van Zalk ◽  
...  

2011 ◽  
Vol 37 (1) ◽  
pp. 17-23 ◽  
Author(s):  
Cui-huan Jiao ◽  
Cui-hong He ◽  
Jian-chen Geng ◽  
Guang-hua Cui

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