Crystal-Structure of Bis(2,2'-6',2'-terpyridine)manganese(II) Bis(triiodide) [Mn(terpy)2](I3)2

1991 ◽  
Vol 44 (2) ◽  
pp. 303 ◽  
Author(s):  
R Bhula ◽  
DC Weatherburn
Keyword(s):  
Crystal Structure ◽  
Transition Metal ◽  
Metal Ions ◽  
Coordination Sphere ◽  
Metal Ion ◽  
Transition Metal Ions ◽  
Triclinic Space Group ◽  
X Ray ◽  
X Ray Crystallography ◽  
Distorted Octahedral

The crystal structure of [ Mn ( terpy )2](I3)2( terpy = 2,2°:6°,2°-terpyridene) has been determined by X-ray crystallography. The crystals are triclinic, space group Pī , a 9.357(4), b 8.600(2), c 24.531(8) Ǻ, α 93.64(2), B 95.58(3), γ 91.52(2)°, Z 2, V 1960(1)Ǻ3. The structure has been refined to a residual R of 0.065 (Rw 0.070). The coordination sphere of the metal ion is distorted octahedral with each terpy ligand coordinated in a meridional fashion. The structure is compared with those of other M( terpy )2n+ complexes formed by first-row transition metal ions.

Synthesis, structure and metal ion coordination of novel benzodiazamacrocyclic ligands bearing pyridyl and picolinate pendant side-arms

2019 ◽  
Vol 43 (38) ◽  
pp. 15072-15086
Author(s):  
Pavel A. Panchenko ◽  
Anastasia D. Zubenko ◽  
Ekaterina Y. Chernikova ◽  
Yuri V. Fedorov ◽  
Anna V. Pashanova ◽  
...  
Keyword(s):  
Nmr Spectroscopy ◽  
Complex Formation ◽  
Transition Metal ◽  
Metal Ions ◽  
Metal Ion ◽  
Transition Metal Ions ◽  
X Ray ◽  
X Ray Crystallography

Complex formation of benzodiazacrown ethers with heavy and transition metal ions was studied using NMR spectroscopy, potentiometry and X-ray crystallography.

The crystal chemistry of (Mn3 +, Fe3+)-substituted andalusites (viridines and kanonaite), (Al1−x−yMn3x+Fe3y+)2 (OǀSiO4): crystal structure refinements, Mössbauer, and polarized optical absorption spectra

1981 ◽  
Vol 155 (1-2) ◽  
Author(s):  
I. Abs-Wurmbach ◽  
K. Langer ◽  
F. Seifert ◽  
E. Tillmanns
Keyword(s):  
Crystal Structure ◽  
Transition Metal ◽  
Optical Absorption ◽  
Metal Ions ◽  
Crystal Chemistry ◽  
Mixed Crystal ◽  
Transition Metal Ions ◽  
Structure Type ◽  
Optical Absorption Spectra ◽  
Distorted Octahedral

AbstractThe crystal chemistry of viridines and kanonaite, (AlThe structure refinements reveal that the transition metal ions substitute for Al almost exclusively in the distorted octahedral Al(l) site of the andalusite structure type within the entire mixed crystal series. This is independently proven by the Mössbauer results for

A new tetradentate N2O2-type Schiff base ligand. Synthesis, extractive properties towards transition metal ions and X-ray crystal structure of its nickel complex

2007 ◽  
Vol 32 (3) ◽  
pp. 374-378 ◽  
Author(s):  
Mohammad Reza Yaftian ◽  
Saeed Rayati ◽  
Reyhaneh Safarbali ◽  
Niloofar Torabi ◽  
Hamid Reza Khavasi
Keyword(s):  
Crystal Structure ◽  
Schiff Base ◽  
Transition Metal ◽  
Metal Ions ◽  
Schiff Base Ligand ◽  
Nickel Complex ◽  
Transition Metal Ions ◽  
X Ray ◽  
Ligand Synthesis

N,N-Disubstituierte Nʹ-Ferrocenoylthioharnstoffe als zweizähnige Komplexliganden für Übergangsmetallionen. Kristallstruktur von Bis-(N,N-diethyl-Nʹ-ferrocenoylthioureato)nickel(II) / N,N-Disubstituted Nʹ-Ferrocenoyl Thioureas as Bidentate Ligands for Transition Metal Ions. Crystal Structure of Bis-(N,N-diethyl-Nʹ-ferrocenoylthioureato)nickel(II)

1995 ◽  
Vol 50 (11) ◽  
pp. 1679-1684 ◽  
Author(s):  
Oliver Seidelmann ◽  
Lothar Beyer ◽  
Rainer Richter
Keyword(s):  
Crystal Structure ◽  
Transition Metal ◽  
Metal Ions ◽  
Transition Metal Ions ◽  
Potassium Thiocyanate ◽  
Bidentate Ligands ◽  
Space Group ◽  
X Ray

N,N-diethyl-Nʹ-ferrocenoyl-thiourea and N-(morpholino-thiocarbonyl)ferrocenecarboxylic amide have been prepared by the reaction of ferrocenoyl chloride with potassium thiocyanate and the respective amine in dry acetone. These bidentate ligands yield neutral heterometalIic complexes with Ni(II), Cu(II), Mn(II) and Co(III). The dark brown air stable crystals of bis-(N,N-diethyl-Nʹ-ferrocenoylthioureato)nickel(II) were characterized by X-ray structure de­termination. Lattice dimensions: a = 1870.9(1), 6= 1161.5(1), c = 1491.4(1) pm; space group Pca21, Z = 4, R = 0.030 for 5707 observed reflections.

The electron-transfer based interaction between transition metal ions and photoluminescent graphene quantum dots (GQDs): A platform for metal ion sensing

Talanta ◽  
2013 ◽  
Vol 117 ◽  
pp. 152-157 ◽  
Author(s):  
Hongduan Huang ◽  
Lei Liao ◽  
Xiao Xu ◽  
Mingjian Zou ◽  
Feng Liu ◽  
...  
Keyword(s):  
Quantum Dots ◽  
Electron Transfer ◽  
Transition Metal ◽  
Metal Ions ◽  
Metal Ion ◽  
Graphene Quantum Dots ◽  
Transition Metal Ions ◽  
Ion Sensing ◽  
Metal Ion Sensing

scholarly journals X-ray crystallographic insights into post-synthetic metalation products in a metal–organic framework

2017 ◽  
Vol 375 (2084) ◽  
pp. 20160028 ◽  
Author(s):  
Michael T. Huxley ◽  
Campbell J. Coghlan ◽  
Witold M. Bloch ◽  
Alexandre Burgun ◽  
Christian J. Doonan ◽  
...  
Keyword(s):  
Transition Metal ◽  
Metal Complexes ◽  
Transition Metal Complexes ◽  
Coordination Sphere ◽  
Metal Organic Frameworks ◽  
Void Space ◽  
X Ray ◽  
X Ray Crystallography ◽  
Metal Nitrates ◽  
Metal Organic

Post-synthetic modification of metal–organic frameworks (MOFs) facilitates a strategic transformation of potentially inert frameworks into functionalized materials, tailoring them for specific applications. In particular, the post-synthetic incorporation of transition-metal complexes within MOFs, a process known as ‘metalation’, is a particularly promising avenue towards functionalizing MOFs. Herein, we describe the post-synthetic metalation of a microporous MOF with various transition-metal nitrates. The parent framework, 1 , contains free-nitrogen donor chelation sites, which readily coordinate metal complexes in a single-crystal to single-crystal transformation which, remarkably, can be readily monitored by X-ray crystallography. The presence of an open void surrounding the chelation site in 1 prompted us to investigate the effect of the MOF pore environment on included metal complexes, particularly examining whether void space would induce changes in the coordination sphere of chelated complexes reminiscent of those found in the solution state. To test this hypothesis, we systematically metalated 1 with first-row transition-metal nitrates and elucidated the coordination environment of the respective transition-metal complexes using X-ray crystallography. Comparison of the coordination sphere parameters of coordinated transition-metal complexes in 1 against equivalent solid- and solution-state species suggests that the void space in 1 does not markedly influence the coordination sphere of chelated species but we show notably different post-synthetic metalation outcomes when different solvents are used. This article is part of the themed issue ‘Coordination polymers and metal–organic frameworks: materials by design’.

Characterization on the Microstructures and Optical Performances of TiO2 Doped with Transition Metals

2014 ◽  
Vol 887-888 ◽  
pp. 388-394 ◽  
Author(s):  
Xin Hua Liu ◽  
Yi Deng ◽  
Yu Chuan Zhang ◽  
Yin Hang Zhou
Keyword(s):  
Transition Metal ◽  
Metal Ions ◽  
Photoelectron Spectroscopy ◽  
Transition Metal Ions ◽  
Ultraviolet Region ◽  
Visible Light Region ◽  
X Ray Diffraction ◽  
X Ray ◽  
Light Region ◽  
Cu Ions

The structures and optical performances of TiO2doped with 4thperiodic transition metal ions were investigated in this paper. The characterization results of X-ray photoelectron spectroscopy and X-ray diffraction showed that the transition metal ions existed in oxidative states, and composites formed because of the reaction between doped metal ions and TiO2. The absorption spectroscopy of TiO2doped with zinc was mainly in ultraviolet region, close to that of the pure TiO2. While for TiO2doped with other transition metal ions including V, Cr, Mn, Fe, Co, Ni and Cu ions, the absorption spectroscopies covered ultraviolet region and visible light region, much broader than that of the pure TiO2.

2,2î-Bipyridine Catalyzed Bleaching of Cotton Fibers with Peracetic Acid

1988 ◽  
Vol 58 (4) ◽  
pp. 198-210 ◽  
Author(s):  
James W. Rucker ◽  
David M. Cates
Keyword(s):  
Transition Metal ◽  
Metal Ions ◽  
Peracetic Acid ◽  
Metal Ion ◽  
Solution Treatment ◽  
Transition Metal Ions ◽  
Ferrous Ion ◽  
Cotton Fibers ◽  
Lauryl Sulfate ◽  
Ferrous Ions

Peracetic acid can be catalyzed to bleach cotton fibers at temperatures as low as 30°C by incorporating 2,2î-bipyridine in the bleach solution. Treatment of the fibers with HCl prior to bleaching reduces bleaching effectiveness by removing trace transition metal ions from the fibers. Sorption of individual ions (Cr+3 Mn+2, Fe+2, Fe+3 Co+2, Ni+2, Cu+2, and Zn+2) by HCl treated cotton fibers prior to bleaching indicates that the ferrous ion produces the greatest catalytic effect, and it is only effective when the metal ion is in the fiber as opposed to in solution. Ferrous ions in the fibers sorb 2,2î-bipyridine from solution to form the tris-2,2î-bipyridine ferrous ion complex that is associated with the fibers, and it is the trischelate associated with the fibers that catalyzes bleaching. The effects of pH, temperature, and concentrations of 2,2î-bipyridine, sodium lauryl sulfate, and transition metal ions (in the fibers and in solution) on bleaching effectiveness and peracetic acid decomposition have been studied, and a bleaching mechanism is proposed.

Intermediate-stage transition metal ion exchange in a zeolite X

1982 ◽  
Vol 35 (7) ◽  
pp. 1335 ◽  
Author(s):  
M Chatterjee ◽  
D Ganguli
Keyword(s):  
Ion Exchange ◽  
Transition Metal ◽  
Metal Ions ◽  
Metal Ion ◽  
Intermediate Stage ◽  
Transition Metal Ions ◽  
Zeolite X ◽  
Counter Ions ◽  
Metal Ion Exchange ◽  
Exchange Behaviour

The exchange behaviour of some divalent transition metal ions M2+ (Zn2+, Cu2+, Ni2+, Co2+, Mn2+) in a zeolite NaX (SiO2/Al2O3 2.75) was studied at intermediate stages before equilibrium. The equivalent counter ion supply in the solution, given by the equivalent ratio of the two counter ions 2M2+/Na+, was found to be critical in determining the saturation level of exchange. The series of relative abilities of exchange was very similar to the well known selectivity series at equilibrium. It is suggested that water exchange of the metal ions in solution could be one of the factors controlling the relative ease of ion exchange.

Interaction of Mixed-Donor Macrocycles Containing the 1,10-Phenanthroline Subunit with Selected Transition and Post-Transition Metal Ions: Metal Ion Recognition in Competitive Liquid−Liquid Solvent Extraction of CuII, ZnII, PbII, CdII, AgI, and HgII

2008 ◽  
Vol 47 (18) ◽  
pp. 8391-8404 ◽  
Author(s):  
M. Carla Aragoni ◽  
Massimiliano Arca ◽  
Andrea Bencini ◽  
Silvia Biagini ◽  
Alexander J. Blake ◽  
...  
Keyword(s):  
Solvent Extraction ◽  
Transition Metal ◽  
Metal Ions ◽  
Metal Ion ◽  
Transition Metal Ions ◽  
Ion Recognition
Sign in / Sign up

Export Citation Format

Share Document