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An entry from the Cambridge Structural Database, the world’s repository for small molecule crystal structures. The entry contains experimental data from a crystal diffraction study. The deposited dataset for this entry is freely available from the CCDC and typically includes 3D coordinates, cell parameters, space group, experimental conditions and quality measures.
A series of core-shell-structured composite molecular sieves comprising zeolite single crystals (i.e., ZSM-5) as a core and ordered mesoporous silica as a shell were synthesized by means of a surfactant-directed sol-gel process in basic medium by using cetyltrimethylammonium bromide (CTAB) as a template and tetraethylorthosilicate (TEOS) as silica precursor. Through this coating method, uniform mesoporous silica shells closely grow around the anisotropic zeolite single crystals, the shell thickness of which can easily be tuned in the range of 15-100 nm by changing the ratio of TEOS/zeolite. The obtained composite molecular sieves have compact meso-/micropore junctions that form a hierarchical pore structure from ordered mesopore channels (2.4-3.0 nm in diameter) to zeolite micropores (≈0.51 nm). The short-time kinetic diffusion efficiency of benzene molecules within pristine ZSM-5 (≈7.88×10(-19) m(2) s(-1)) is almost retainable after covering with 75 nm-thick mesoporous silica shells (≈7.25×10(-19) m(2) s(-1)), which reflects the greatly opened junctions between closely connected mesopores (shell) and micropores (core). The core-shell composite shows greatly enhanced adsorption capacity (≈1.35 mmol g(-1)) for large molecules such as 1,3,5-triisopropylbenzene relative to that of pristine ZSM-5 (≈0.4 mmol g(-1)) owing to the mesoporous silica shells. When Al species are introduced during the coating process, the core-shell composite molecular sieves demonstrate a graded acidity distribution from weak acidity of mesopores (predominant Lewis acid sites) to accessible strong acidity of zeolite cores (Lewis and Brønsted acid sites). The probe catalytic cracking reaction of n-dodecane shows the superiority of the unique core-shell structure over pristine ZSM-5. Insight into the core-shell composite structure with hierarchical pore and graded acidity distribution show great potential for petroleum catalytic processes.
An entry from the Cambridge Structural Database, the world’s repository for small molecule crystal structures. The entry contains experimental data from a crystal diffraction study. The deposited dataset for this entry is freely available from the CCDC and typically includes 3D coordinates, cell parameters, space group, experimental conditions and quality measures.
The book Recent Progress in Organometallic Chemistry mostly reviews the modem techniques and substantial organometallic and medical applications of inorganic materials. Chapters of this book are invited and contributed from the experts throughout the world from prominent researchers and scientists in the field of inorganic chemistry on organometallics and metallocenes. Each chapter provides technical and methodological details beyond the level found in typical journal articles or reviews and explores the application of organometallics, medicinal, inorganic, and catalysis to a significant problem in medical and catalysis, also providing a prospectus for the future. This book compiles with the expert knowledge of many specialists in the organic-inorganic synthesis and use of inorganic catalyst and metallocenes including chemical catalysis, biological catalysis, photo-electrocatalysis, bioassays, industrial catalysis, large-scale synthesis, micro-nanocatalyst, and so on in the field of fundamental and applied organometallic chemistry. Highlighting and importance are included on real and practical problems, ranging from industrial to medical applications and from single-multicells to animal to human objects. This offers the unique opportunity of exchanging and combining the scientist or researcher in organometallic chemistry in largely chemistry, biological, biomedical, physiological, metallocene, and inorganic chemistry fields.
Abstract C 40 H 26 N 4 , triclinic, P 1̄ (no. 2), a = 9.5201(6) Å, b = 12.1701(8) Å, c = 12.8721(7) Å, α = 79.949(5)°, β = 88.350(5)°, γ = 75.893(6)°, V = 1424.05(16) Å 3 , Z = 2, R gt ( F ) = 0.0519, wR ref ( F 2 ) = 0.1403, T = 293 K.