Document Type: Article All Authors / Contributors: Wakefield B.; Goudy A.; Orefuwa S.; Lott L.Q.; Alexander D.; Kerr A. ISSN:0065-7727 Language Note: English Unique Identifier: 794408421 Awards:
| Title | : | Synthesis of new naphthalene linkers for incorporation in hydrogen storing metal organic frameworks |
| Author | : | Wakefield B.; Goudy A.; Orefuwa S.; Lott L.Q.; Alexander D.; All authors |
| Language | : | en |
| Rating | : | 4.90 out of 5 stars |
| Type | : | PDF, ePub, Kindle |
| Uploaded | : | Apr 12, 2021 |
Download Synthesis of new naphthalene linkers for incorporation in hydrogen storing metal organic frameworks - Wakefield B.; Goudy A.; Orefuwa S.; Lott L.Q.; Alexander D.; All authors file in ePub
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Apr 24, 2018 naphthalene diimide (ndi) dimers, ndi–ph–ndi with a phenyl linker and ndi–xy –ndi with a xylene linker, are designed and synthesized. High‐performance ternary polymer solar cells enabled by a new narrow.
Sep 18, 2018 synthesis of a stable large-pore zr-based metal−organic. Metal−organic frameworks (mofs) are a new generation of sulfonaphthalene-2,6-dicarboxylate (hsndc2−) as the linker.
Carbon can form covalent bonds with itself and other elements to create a mind-boggling array of structures. In organic chemistry, we will learn about the reactions chemists use to synthesize crazy carbon based structures, as well as the analytical methods to characterize them.
The research efforts on oligoacene systems are still relatively limited mainly due to the synthetic challenge and the extreme instability of longer acenes.
Naphthalene-1,2-oxide (npo), 1,2-naphthoquinone (1,2-npq) and 1,4-naphthoquinone (1,4-npq) are the major metabolites of naphthalene that are thought to be responsible for the cytotoxicity and genotoxicity of this chemical. We measured cysteinyl adducts of these metabolites in hemoglobin (hb) and albumin (alb) from f344 rats dosed with 100-800.
Here, we have developed a series of new 1,1′-binaphthalene analogues that efficiently form dna icls upon 350 nm irradiation via generated 2-naphthalenylmethyl cations. The dna cross-linking efficiency depends on the substituents at position 4 of the naphthalene moiety as well as the leaving groups.
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