Synthesis and Crystal Structure of Ulm-16, A New Open Framework Fluorinated Gallium Phosphate with 16-Ring Channels

1996 ◽  
Vol 431 ◽  
Author(s):  
Thierry Loiseau ◽  
Gérard Férey

AbstractThe synthesis and characterization of ULM-16, a new fluorinated gallophosphate Ga4(PO4)F2 • 1.5 NC6H14 • 0.5 H2O • 0.5 H3O, is described. This material is hydrothermally prepared at 180°C using cyclohexylamine as the structuring agent. It cristallizes in the orthorhombic space group Pbcn (n° 60) with a = 27.329(4) Å, b = 17.377(2) Å, c = 10.2124(5) Å, V = 4849.6 (9) Å3 and Z = 8. The structure is built up from vertex-linked GaO4 and PO4 tetrahedra, GaO4F trigonal bipyramids and GaO4F2 octahedra forming hexameric units and infinite double crankshaft chains (called cc or UUDD). The hexameric unit is similar to that found in ULM-3, ULM-4, ULM-5 and ULM-8. The two types of building units are fully connected by vertex-sharing with respect to a strict Ga-P alternation. The 3-D framework consists of cylindrical tunnels delimited by sixteen and six polyhedra running along [001]. The cyclohexylamine molecules are trapped in the wider pores and interact with the bridging fluorine atoms and hydration water through hydrogen bonds. The ULM-16 topology is closely related to that of ULM-5 where, in ULM-16, the infinite crankshaft chains replace the isolated D4R cages of ULM-5. TGA curve (under argon) indicates that the ULM-16 structure is intact up to 800°C. Structural relationships will be stated explicitly for the different structures of the ULM-n series containing the hexameric units.

2018 ◽  
Vol 47 (26) ◽  
pp. 8779-8786 ◽  
Author(s):  
S. Spirkl ◽  
M. Grzywa ◽  
D. Volkmer

The synthesis and crystal structure of a novel metal organic framework, constructed from MnIII, the 4,4′-Bipyrazolate (BPZ) ligand and bridging hydroxyl groups is presented in this work.


2011 ◽  
Vol 66 (6) ◽  
pp. 553-558 ◽  
Author(s):  
Mathias O. Senge ◽  
Monica Pintea ◽  
Aoife A. Ryan

We report the synthesis and characterization of a meso-meso directly linked bisporphyrin 6 bearing both alkyl and aryl residues. Its oxidative fusing results in the corresponding meso-meso β -β ,β -β - linked bisporphyrin. The first crystal structure analysis of a meso-meso directly linked porphyrin dimer (6) has shown the inequivalency of the two porphyrin units with regard to the macrocycle conformation. Quite distinct mixings of distortion modes were observed for the two aromatic macrocycles.


2010 ◽  
Vol 2010 ◽  
pp. 1-7 ◽  
Author(s):  
K. C. Prousis ◽  
G. Athanasellis ◽  
V. Stefanou ◽  
D. Matiadis ◽  
E. Kokalari ◽  
...  

The synthesis and characterization of two new tetronic acid zinc (II) complexes of the empirical formulae [Zn(L–H)2(H2O)2] (1) and [Zn(L–H)2(H2O)(MeOH)]H2O(2) found within the same crystal are reported. The zinc ions bind through alkoxide and carbonyl groups of the ligand 3-methoxycarbonyl-5-phenyl tetronic acid (LH) as indicated byHNMR and X-ray crystallographic studies. These complexes promote intra- and intermolecular interactions, such as hydrogen bonding andπstacking, giving place to the formation of molecular aggregates.


2004 ◽  
Vol 68 (4) ◽  
pp. 677-686 ◽  
Author(s):  
U. Kolitsch ◽  
E. Tillmanns

AbstractDuring investigations of the system Sc2O3-Al2O3-TiO2-SiO2, a new, unusual microporous compound, Cs3ScSi8O19, was synthesized as colourless plates from a CsF-MoO3 flux. The crystal structure was determined from single-crystal X-ray diffraction data (Mo-Kα radiation, CCD area detector). The compound is orthorhombic, space group Pnma, with a = 11.286(2), b = 7.033(1), c = 26.714(5) Å, and Z = 4 (R1(F) = 2.6% and wR2all(F2) = 7.3%, using 3066 ‘observed’ reflections with Fo > 4σ(Fo)). The crystal structure of Cs3ScSi8O19 represents a new microporous framework structure type (‘MCV-1’), and the compound is exceptional in being the first representative of a mixed octahedral-tetrahedral framework structure, in which the [TO4]:[MO6] ratio is >6:1. The structure is based on isolated, nearly regular ScO6 octahedra [dav(Sc—O) = 2.112 Å] sharing corners with SiO4 tetrahedra to form an open framework with four-, six- and eight-membered rings; the latter are formed by SiO4 tetrahedra only. Two fully occupied Cs positions are located in large framework voids close to the six-membered rings, whereas four partly occupied and disordered Cs positions are close to very large framework voids bordered by the puckered eight-membered rings. The cavities are linked into channels parallel to [100] and [010]. The structure is compared with that of Cs2TiSi6O15 and related microporous scandium-, REE-, titano- and zirconosilicate minerals and compounds. Cs3ScSi8O19 or derivatives may be important in the context of immobilization of radioactive 137Cs waste, cationic conductivity or catalysis.


2017 ◽  
Vol 72 (3) ◽  
pp. 215-223
Author(s):  
Teresa S. Ortner ◽  
Daniel Schildhammer ◽  
Martina Tribus ◽  
Bastian Joachim ◽  
Hubert Huppertz

AbstractThree novel mixed alkali borate-nitrates Na3−xKx[B6O10]NO3(x=0.5, 0.6, 0.7) were synthesized hydrothermally; their crystal structures were determined through Rietveld analyses, and supported through EDX as well as vibrational spectroscopy. The phases represent solid solutions of the alkali borate-nitrate Na3(NO3)[B6O10], which was reported in 2002 as a “New type of boron-oxygen framework in the Na3(NO3)[B6O10] crystal structure” (O. V. Yakubovich, I. V. Perevoznikova, O. V. Dimitrova, V. S. Urusov,Dokl. Phys.2002,47, 791). Only two of the three crystallographically independent Na+positions in the new structures are partially substituted by K+; a pure potassium borate-nitrate was not formed until now. The cell parameters of the novel phases vary froma=1261.72(5)–1267.12(5),b=1004.19(5)–1007.96(4),c=770.55(3)–774.38(3) pm, andV=0.97630(6)–0.98905(6) nm3in the orthorhombic space groupPnma(no. 62), in alignment with increasing K+content.


2004 ◽  
Vol 689 (11) ◽  
pp. 1872-1875 ◽  
Author(s):  
José Ruiz ◽  
Consuelo Vicente ◽  
Venancio Rodrı́guez ◽  
Natalia Cutillas ◽  
Gregorio López ◽  
...  

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