“…The existence of terminal Cl atoms and −OH groups leads to a porous sheets containing four-and eight-membered rings within [Zn(HPO 4 )Cl] − layers. Compared to other metalphosphates, these layers can be related to the structure type 488, which was previously seen in many zincophosphates [20,35,36], aluminophosphates (AlPO-12) [37] and gallophosphates (GaPO 4 -14) [38]. Upon heating, this new zincophosphate is stable until 530 K. It undergoes a reversible phase transition at 433 K, the loss of H 2 O molecule at 542 K while the loss of HCl and 4-methylpiperidine molecules occurs between 570 K and 775 K. Above 775 K, the resulting amorphous material is Zn 2 P 2 O 7 characterized elsewhere.…”
A chlorozincophosphate with the composition Zn(HPO 4 )Cl .[C 6 H 14 N] has been synthesised under mild conditions in water medium in presence of 4-methylpiperidine as organic template. The structure was determinated by single crystal X-ray diffraction. The unit cell is orthorhombic (space group Pcab) with a = 8.743(9), b = 9.592(6), c = 26.573(6) Å, Z = 8 and V = 2228.91(12) Å 3 . The structure involves a network of ZnO 3 Cl and PO 3 (OH) tetrahedra forming macroanionic inorganic layers with four and eight-membered rings. Charge balance is achieved by the protonated amine which is trapped in the interlayers space and interacts with the organic framework through hydrogen bonding. Solid state 31 P and 13 C MAS-NMR spectroscopies are in full agreement with the X-ray structure.
“…The existence of terminal Cl atoms and −OH groups leads to a porous sheets containing four-and eight-membered rings within [Zn(HPO 4 )Cl] − layers. Compared to other metalphosphates, these layers can be related to the structure type 488, which was previously seen in many zincophosphates [20,35,36], aluminophosphates (AlPO-12) [37] and gallophosphates (GaPO 4 -14) [38]. Upon heating, this new zincophosphate is stable until 530 K. It undergoes a reversible phase transition at 433 K, the loss of H 2 O molecule at 542 K while the loss of HCl and 4-methylpiperidine molecules occurs between 570 K and 775 K. Above 775 K, the resulting amorphous material is Zn 2 P 2 O 7 characterized elsewhere.…”
A chlorozincophosphate with the composition Zn(HPO 4 )Cl .[C 6 H 14 N] has been synthesised under mild conditions in water medium in presence of 4-methylpiperidine as organic template. The structure was determinated by single crystal X-ray diffraction. The unit cell is orthorhombic (space group Pcab) with a = 8.743(9), b = 9.592(6), c = 26.573(6) Å, Z = 8 and V = 2228.91(12) Å 3 . The structure involves a network of ZnO 3 Cl and PO 3 (OH) tetrahedra forming macroanionic inorganic layers with four and eight-membered rings. Charge balance is achieved by the protonated amine which is trapped in the interlayers space and interacts with the organic framework through hydrogen bonding. Solid state 31 P and 13 C MAS-NMR spectroscopies are in full agreement with the X-ray structure.
“…Since the discovery of first microporous zinc phosphates with zeolite-like topologies by Stucky and co-workers, a large number of zinc phosphates have been synthesized in the presence of organic, as well as inorganic templates. – ,,,,,,– …”
Section: Framework Phosphatesmentioning
confidence: 99%
“…It is difficult to discuss all the 2D structure types (see Table ), and we will limit ourselves to a few typical ones. Among the structures with strictly alternating ZnO 4 and PO 4 tetrahedra, the commonly found one is that with a Zn/P ratio of 2/3 where a 12-membered bifurcated aperture is formed when the HPO 4 groups cross-link zigzag ladders (Figure b). ,,,, Then, there are also structures with 4.8 ,,, and 4.6.8 nets. Among the sheet structures with a tricoordinated oxygen, a stoichiometry of Zn 6 (HPO 4 ) 2 (PO 4 ) 4 with a Zn/P ratio of unity is the most common ,,,,, (Figure ).…”
“…Natarajan et al [26][27][28] have recently used hydrochloric acid as a mineraliser in the preparation of a number of zinc phosphates with a range of dimensionalities but, as is observed here, no Cl was incorporated into the final ZnPO products. However, chlorinated ZnPOs [TH][Zn(HPO 4 )Cl] (T = cyclohexylamine [29], piperidine [30] and 1,6-diaminohexane [31]) and [TH] 2 [Zn(HPO 4 ) 2 Cl 2 ] (T = cyclohexylamine [32]), have also been prepared in the presence of HCl. All have layered structures assembled from ZnO 3 Cl and PO 4 tetrahedra.…”
A new 3-D zinc phosphate, [C 5 N 2 H 14 ][Zn 2 (PO 3 (OH)) 3 ], has been synthesised under solvothermal conditions in the presence of 1-methylpiperazine. The structure, determined by single-crystal X-ray diffraction at 293 K (RMM = 520.9, orthorhombic, space group P2 1 2 1 2 1 ; a = 10.0517(2) Å, b =10.4293(2) Å and c = 14.9050(5) Å; V = 1562.52 Å 3 ; Z = 4; R(F) = 2.60%, wR(F) = 2.93%), consists of vertex linked ZnO 4 and PO 3 (OH) tetrahedra assembled into (4.8) net sheets which in turn are linked through further PO 3 (OH) units to generate a 3-D framework. 1-Methylpiperazinium cations reside within the 3-D channel system, held in place by a strong network of hydrogen bonds. The (4.8) net sheets occur in a number of zeolite structures e.g. ABW and GIS and related zinc phosphate phases. To cite this articles: F.
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