2009
DOI: 10.1021/cm802981m
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Rapid Microwave Synthesis and Purification of Porous Covalent Organic Frameworks

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Cited by 391 publications
(263 citation statements)
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“…47,48 These attributes, along with higher product yields and improved chemical selectivity, make microwave assisted techniques inherently green compared to conventional heating techniques. The use of microwave energy to heat and drive chemical reactions is growing at a rapid rate, with new and innovative applications in material sciences, [49][50][51] and nanotechnology. 52,53 Irradiation of a semiconductor with light of energy equal to or larger than the bandgap energy leads to the generation of electron-hole pairs, which can subsequently induce redox reactions on the semiconductor.…”
Section: Introductionmentioning
confidence: 99%
“…47,48 These attributes, along with higher product yields and improved chemical selectivity, make microwave assisted techniques inherently green compared to conventional heating techniques. The use of microwave energy to heat and drive chemical reactions is growing at a rapid rate, with new and innovative applications in material sciences, [49][50][51] and nanotechnology. 52,53 Irradiation of a semiconductor with light of energy equal to or larger than the bandgap energy leads to the generation of electron-hole pairs, which can subsequently induce redox reactions on the semiconductor.…”
Section: Introductionmentioning
confidence: 99%
“…1b using a trivalent 1,3,5-triazine connecting group. 2D COFs can now be synthesized using dynamic covalent chemistry in milligram quantities 9 organic monomers, with solvothermal 10 , microwave 11,12 and ionothermal 13,14 synthesis in solution or directly as monolayers on metallic 15 and graphitic 16,17 substrates. Solution-based monoand few-layer sheets can now be produced at micron diameters, highly crystalline 18 and largely defect-free 19 .…”
mentioning
confidence: 99%
“…Cooper and coworkers prepared porous covalent organic frameworks (COFs) from a 3:2 molar ratio solution of 1,4-benzenediboronic acid (BDBA) and 2,3,6,7,10,11-hexahydroxytriphenylene (HHTP) in a 1:1 mixture of mesitylene and 1,4-dioxane. [83] The mixture was sealed under an inert atmosphere of nitrogen and exposed to microwave irradiation in a single-mode CEM SClass Explorer microwave reactor at 100 8C for 20 min. It was found that the microwave-assisted synthesis of COFs was about 200 times faster than solvothermal synthesis.…”
Section: Polymerizations Involving Càc Coupling Reactionsmentioning
confidence: 99%