Method for manufacturing a bevelled stone, particularly for a horological movement
US-2022365487-A1 · Nov 17, 2022 · US
US11479470B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11479470-B2 |
| Application number | US-201716077415-A |
| Country | US |
| Kind code | B2 |
| Filing date | Feb 21, 2017 |
| Priority date | Feb 18, 2016 |
| Publication date | Oct 25, 2022 |
| Grant date | Oct 25, 2022 |
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Novel three-dimensional molecular clusters and methods of their synthesis are provided. The three-dimensional molecular clusters may be perfunctionalized polyhedral boranes and carboranes. The three-dimensional clusters may be configured to manipulate the photophysical properties of other materials, including, for example, for use as photooxidants or as components in organic light-emitting diode materials. Methods are also provided for synthesizing and perfunctionalizing such three-dimensional clusters. The three-dimensional clusters may also be configured for use as organomimetic materials.
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What is claimed is: 1. A metal-free photooxidant comprising an icosahedral dodecaborate consisting of B 12 (OR) 12 , where R is a substituent selected from the group consisting of CH 2 C 6 F 5 , CH 2 (4-CF 3 C 6 H 4 ), and CH 2 (3,5-(CF 3 ) 2 C 6 H 3 ). 2. A molecular scaffold for forming atomically precise nanomolecules comprising an icosahedral dodecaborate of B 12 (OR) 12 , where R is a perfluoroaryl terminated linker. 3. The molecular scaffold of claim 2 , wherein the dodecaborate is perfunctionalized with one or more substituted aromatic perfunctionalization groups, and each of the perfluoraryl terminated linkers is attached to the dodecaborate through said perfunctionalization groups. 4. The molecular scaffold of claim 2 , wherein one or more of the fluorine atoms of the perfluoroaryl terminated linkers is substituted with a thiol-containing molecule or macromolecule. 5. The molecular scaffold of claim 4 , wherein the thiol-containing macromolecule is a peptide such that the molecular scaffold is an organomimetic cluster nanomolecule. 6. The molecular scaffold of claim 2 , wherein the molecular scaffold is PEGylated. 7. The molecular scaffold of claim 4 , wherein the thiol-containing molecule is a recognition moiety. 8. The molecular scaffold of claim 7 , wherein the recognition moieties are glycoconjugates. 9. The molecular scaffold of claim 8 , wherein the glycoconjugates are linked with one or more molecules selected from the group consisting of proteins, peptides, lipid and saccharides. 10. The molecular scaffold of claim 7 , wherein the molecular scaffold forms an organomimetic cluster nanomolecule that functions as one of an antibody, protein, histone or viral mimic. 11. The molecular scaffold of claim 10 , wherein the molecular scaffold further comprises a viral scaffold and at least one fluorescent moiety, and wherein the molecular scaffold operates as a viral assay. 12. The molecular scaffold of claim 11 , wherein the viral scaffold is a gp41 viral scaffold. 13. The molecular scaffold of claim 10 , wherein the histone mimic comprises a periodic arrangement of cationic lysine residues separated by one or more helix-promoting hydrophobic amino acids.
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