Heterocyclic compounds can be divided into two categories: alicyclic heterocycles and aromatic heterocycles. Compounds whose heterocycles in the molecular skeleton cannot reflect aromaticity are called alicyclic heterocyclic compounds. Compound: 111-18-2, is researched, Molecular C10H24N2, about Molecular level nucleation mechanisms of hierarchical MFI and MOR zeolite structures via non-stochastic pathways, the main research direction is aluminum sodium oxide silica mol structure recognition PXRD spectrum.COA of Formula: C10H24N2.
Understanding the chem. mechanism of crystal nucleation at the mol. level is crucial for the design of architectural structures of valuable materials in the future. In this study, it has been revealed that amorphous silicate precursors, which play a role in the nucleation processes of zeolitic frameworks, can be regularly fragmented in mass spectroscopy due to the hydroxyl functional groups in their mol. structures. In this way, by using the mass spectra acquired from LDI-TOF MS, the systematic evolution stages of a common 1D precursor converting to the 3D unit cells of MFI and MOR zeolite structures observed in the same reaction medium were constructed through a nucleation mechanism at the mol. level for the first time. Here we show a novel nucleation pathway that does not occur via stochastic assembly of atoms or distinct building blocks by mol. recognition. Each of the proposed nucleation mechanisms of these different frameworks carrying structural similarities is from different combinations of sequential self-attaching intramol. covalent couplings of identical origin precursors. The dynamic mol. structure capable of forming finite building units of target frameworks during the nucleation process of this precursor, which is the polymerized form of simple 6-membered siloxane chains, has been arranged around structure directing agents before a hydrothermal reaction.
After consulting a lot of data, we found that this compound(111-18-2)COA of Formula: C10H24N2 can be used in many types of reactions. And in most cases, this compound has more advantages.
Reference:
Thiazole | C3H3NS – PubChem,
Thiazole | chemical compound | Britannica