“…All these findings are supported by quantum-chemical calculations [15] and are in agreement with data published elsewhere [12].…”
Section: Resultssupporting
confidence: 92%
“…19 F NMR chemical shifts were detected in the region of those reported for Xe(C 6 F 5 ) 2 [8][9][10] and Xe(2,4,6-F 3 C 6 H 2 ) 2 [12], significantly shifted from those of salt-like fluorophenylxenon derivatives (e.g. [6,12,16,17]). The same can be applied in a somewhat less significant manner with respect to 2,6-difluorophenylxenon compounds.…”
Section: Resultsmentioning
confidence: 72%
“…In a recent publication [12] Frohn and Theißen proved the existence of 2,4,6-F 3 C 6 H 2 XeC 6 F 5 and Xe(2,4,6-F 3 C 6 H 2 ) 2 by 19 F and 129 Xe NMR spectroscopic means and supported their results by theoretical calculations.…”
Section: Introductionmentioning
confidence: 72%
“…Cadmium reagents were also employed in the syntheses of 2,4,6-F 3 C 6 H 2 XeC 6 F 5 and Xe(2,4,6-F 3 C 6 H 2 ) 2 [12].…”
Section: Resultsmentioning
confidence: 99%
“…While ligand exchange reactions with less or low co-ordinating anions have been a major part of investigations [3][4][5][6][7], attempts to prepare hypervalent [10-Xe-2] remained of lower success [8][9][10][11][12].…”
“…All these findings are supported by quantum-chemical calculations [15] and are in agreement with data published elsewhere [12].…”
Section: Resultssupporting
confidence: 92%
“…19 F NMR chemical shifts were detected in the region of those reported for Xe(C 6 F 5 ) 2 [8][9][10] and Xe(2,4,6-F 3 C 6 H 2 ) 2 [12], significantly shifted from those of salt-like fluorophenylxenon derivatives (e.g. [6,12,16,17]). The same can be applied in a somewhat less significant manner with respect to 2,6-difluorophenylxenon compounds.…”
Section: Resultsmentioning
confidence: 72%
“…In a recent publication [12] Frohn and Theißen proved the existence of 2,4,6-F 3 C 6 H 2 XeC 6 F 5 and Xe(2,4,6-F 3 C 6 H 2 ) 2 by 19 F and 129 Xe NMR spectroscopic means and supported their results by theoretical calculations.…”
Section: Introductionmentioning
confidence: 72%
“…Cadmium reagents were also employed in the syntheses of 2,4,6-F 3 C 6 H 2 XeC 6 F 5 and Xe(2,4,6-F 3 C 6 H 2 ) 2 [12].…”
Section: Resultsmentioning
confidence: 99%
“…While ligand exchange reactions with less or low co-ordinating anions have been a major part of investigations [3][4][5][6][7], attempts to prepare hypervalent [10-Xe-2] remained of lower success [8][9][10][11][12].…”
The trifluoromethyl and perfluoroalkyl functional groups possess significant thermal, chemical, and metabolic stability, as well as high lipophilicity and electronegativity. These physicochemical properties render fluorinated carbon residues indispensable in diverse applications, such as agrochemistry, drug design, and material chemistry. The generation and properties of nucleophilic perfluoroalkyl reagents as well as the scope and limitations of their additions to various electrophilic partners is described in this chapter.
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