215500-01-9

Upstream product

• 13709-36-9 xenon difluoride 
• 830-49-9 difluoro (pentafluorophenyl)borane 
• 830-48-8 dichloro(pentafluorophenyl)borane 
• 123168-24-1 {acetonitrile(pentafluorphenyl)xenon(II)}{(C₆F₅)2BF₂} 
• 7637-07-2 boron trifluoride 
• 260405-66-1 pentafluorophenyldifluoroxenonium(IV) tetrafluoroborate 
• 827-15-6 1,2,3,4,5-pentafluoro-6-iodobenzene 
• 7553-56-2 iodine 
• 1259-35-4 tris(pentafluorophenyl)phosphine 
• 123168-25-2 (C₆F₅Xe)⁽¹⁺⁾*{(C₆F₅)2BF₂}^(1-) = (C₆F₅Xe){(C₆F₅)2BF₂} 

Downstream Products

• 1019339-56-0 [C₆F₅Xe]⁽¹⁺⁾*[B(CF₃)4]^(1-)=[C₆F₅Xe][B(CF₃)4] 
• 1019339-58-2 [C₆F₅Xe]⁽¹⁺⁾*[B(CN)4]^(1-)=[C₆F₅Xe][B(CN)4] 
• 1019339-57-1 [C₆F₅XeNCCH₃]⁽¹⁺⁾*[B(CF₃)4]^(1-)=[C₆F₅XeNCCH₃][B(CF₃)4] 
• 958452-11-4 [(C₆F₅)Xe(acetonitrile)]B(C₆F₅)4 
• 319439-13-9 (p-fluorophenyl)(pentafluorophenyl)iodonium tetrafluoroborate 
• 249733-81-1 pentafluorophenylxenon(II) chloride 
• 420-16-6 acetonitrile boron trifluoride complex 
• 358-43-0 triethylsilyl fluoride 
• 358-06-5 diethylsilyl difluoride 
• 328379-54-0 bis(pentafluorophenyl)xenon 
• 363-72-4 Pentafluorobenzene 
• 686-70-4 diethylfluorosilane 
• 2251-81-2 ethylpentafluorobenzene 
• 328379-53-9 (pentafluorophenyl)fluoroxenon(II) 

Relevant academic research and scientific papers

(Fluoroorgano)fluoroboranes and -borates. 7 [1]. The reaction of RFBF2 and K [RFBF3] (RF = perfluorophenyl-, perfluoroalk-1-enyl- and perfluoroalkyl) with xenon difluoride in anhydrous HF

The dissolution of (perfluoroorgano)difluoroboranes RFBF2 in anhydrous HF (aHF) resulted in equilibrium mixtures of the starting borane and different kinds of acid-base products: [H2F] [RFBF2(F · HF)]

Syntheses, solution multi-NMR characterization, and reactivities of [C 6F5Xe]+ salts of weakly coordinating borate anions, [BY4]- (Y = CF3, C6F 5, CN, or OTeF5

New examples of [C6F5Xe]+ salts of the weakly coordinating anions [B(CF3)4]_, [B(C6F5)4]-, [B(CN) 4]-, and [B(OTeF5/s

A Simple and Convenient Route to Arylxenon(II) Tetrafluoroborates

An improved synthesis of arylxenon(II) salts is reported. The series of fluoro-containing arylxenon(II) tetrafluoroborates (aryl = C6F5, 2,3,4,5-C6HF4, 3,4,5-C6H2F3 and 3,5-C6H3F2) are prepared by the reaction of xenon difluoride with the corresponding aryldifluoroboranes. The salts [C6F5Xe] [BF4] and [2,3,4,5-C6HF4Xe] [BF4] are long-term stable in anhydrous HF (aHF) solution at rt, while [3,4,5-C6H2F3Xe] [BF4] and [3,5-C6H3F2Xe] [BF4] are converted into 1,2,3,5-tetrafluorobenzene and 1,3,5-trifluorobenzene, respectively, within a few hours.