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HPM - 3的结构与相变:一种具有拓扑结构的中性磷酸铝层状前驱体

Structure, and Phase Transformations of HPM-3: A Layered Precursor of the Neutral Aluminophosphate with Topology.

作者信息

Yu Huajian, Kim Eun Jeong, Gao Zihao Rei, Lee Jeong Hwan, Balestra Salvador R G, Ma Chao, Li Jian, Márquez-Álvarez Carlos, Marler Bernd, Hong Suk Bong, Camblor Miguel A

机构信息

Instituto de Ciencia de Materiales de Madrid (ICMM), CSIC, Madrid 28049, Spain.

Center for Ordered Nanoporous Materials Synthesis, Division of Environmental Science and Engineering, POSTECH, Pohang 37673, Korea.

出版信息

Inorg Chem. 2024 Dec 23;63(51):24429-24439. doi: 10.1021/acs.inorgchem.4c04881. Epub 2024 Dec 9.

DOI:10.1021/acs.inorgchem.4c04881
PMID:39652748
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11918533/
Abstract

The structure of HPM-3, a layered aluminophosphate prepared using 1,2,3-trimethylimidazolium (123TMI) as an organic structure-directing agent by the fluoride route, has been solved by continuous rotation electron diffraction (cRED), and Rietveld refined against synchrotron powder X-ray diffraction data. Charge balance of the occluded cation is achieved through F anions and dangling Al(OP)OH groups. Half of the Al is pentacoordinated in negatively charged Al(OP)-F-Al(OP) pairs. The layers in HPM-3, denoted as , are observed in the fully connected metalloaluminophosphate molecular sieves with topology. Thus, HPM-3 can be a precursor to a metal-free aluminophosphate if a topotactic condensation can be reached, which proved to be difficult but feasible. Treatments under different conditions resulted in a number of known (PST-27 and AlPO-5 by a disruptive transformation) or new phases (through mild thermal treatments). Among the latter, a layered phase with a shorter interlayer space, denoted as HPM-3S, contains half the amount of organic as HPM-3. This is afforded by the capability of 123TMI compounds to sublimate at relatively low temperatures. HPM-3S still contains the same layers. Therefore, the transformation of HPM-3 into HPM-3S is topotactic but without reaching condensation. Among the phases appearing under calcination conditions at relatively low temperature (<350 °C), we observed solids compatible with the topology, but with poor crystallinity. This is attributed to a wrong alignment in HPM-3 of the dangling Al(OP)OH and P(OAl)═O that should connect adjacent layers in a topotactic condensation, which favors 1-dimensional stacking disorder by random shifts of layers during the thermal treatments. However, detemplation at a much lower temperature (175 °C) using O finally afforded an aluminophosphate molecular sieve with topology with only moderate stacking disorder. This is just the third reported 2D-to-3D topotactic condensations in aluminophosphates.

摘要

HPM - 3是一种层状铝磷酸盐,通过氟化物路线使用1,2,3 - 三甲基咪唑鎓(123TMI)作为有机结构导向剂制备而成。其结构已通过连续旋转电子衍射(cRED)解析,并根据同步加速器粉末X射线衍射数据进行了Rietveld精修。通过F阴离子和悬挂的Al(OP)OH基团实现了包藏阳离子的电荷平衡。一半的Al以带负电荷的Al(OP)-F-Al(OP)对的形式五配位。HPM - 3中的层,记为 ,在具有 拓扑结构的完全连接的金属铝磷酸盐分子筛中被观察到。因此,如果能实现拓扑缩合,HPM - 3可以成为无金属铝磷酸盐的前体,事实证明这虽然困难但可行。在不同条件下进行处理会产生许多已知相(通过破坏性转变得到PST - 27和AlPO - 5)或新相(通过温和热处理)。在后者中,一种层间间距较短的层状相,记为HPM - 3S,其有机含量是HPM - 3的一半。这是由123TMI化合物在相对较低温度下升华能力所致。HPM - 3S仍然包含相同的 层。因此,HPM - 3向HPM - 3S的转变是拓扑的,但未达到缩合。在相对较低温度(<350 °C)的煅烧条件下出现的相中,我们观察到与 拓扑结构兼容但结晶度较差的固体。这归因于HPM - 3中悬挂的Al(OP)OH和P(OAl)═O的排列错误,它们应在拓扑缩合中连接相邻层,这有利于在热处理过程中通过层的随机移动形成一维堆积无序。然而,在更低温度(175 °C)下使用O进行脱模板最终得到了具有 拓扑结构且堆积无序程度适中的铝磷酸盐分子筛。这是铝磷酸盐中报道的第三次二维到三维拓扑缩合。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bcf6/11918533/adc1a89def8a/ic4c04881_0010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bcf6/11918533/41aa8f54c09e/ic4c04881_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bcf6/11918533/2c0ee664b72c/ic4c04881_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bcf6/11918533/1dc447386d6e/ic4c04881_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bcf6/11918533/b91a72bfec58/ic4c04881_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bcf6/11918533/ab7144d4a280/ic4c04881_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bcf6/11918533/92308388cb8a/ic4c04881_0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bcf6/11918533/2a8d74fcc484/ic4c04881_0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bcf6/11918533/3793a3b6caf0/ic4c04881_0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bcf6/11918533/c4e3f01a6497/ic4c04881_0009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bcf6/11918533/adc1a89def8a/ic4c04881_0010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bcf6/11918533/41aa8f54c09e/ic4c04881_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bcf6/11918533/2c0ee664b72c/ic4c04881_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bcf6/11918533/1dc447386d6e/ic4c04881_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bcf6/11918533/b91a72bfec58/ic4c04881_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bcf6/11918533/ab7144d4a280/ic4c04881_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bcf6/11918533/92308388cb8a/ic4c04881_0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bcf6/11918533/2a8d74fcc484/ic4c04881_0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bcf6/11918533/3793a3b6caf0/ic4c04881_0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bcf6/11918533/c4e3f01a6497/ic4c04881_0009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bcf6/11918533/adc1a89def8a/ic4c04881_0010.jpg

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