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Tungsten(VI) fluoride, also known as tungsten hexafluoride, is an inorganic compound with the formula W F 6.It is a toxic, corrosive, colorless gas, with a density of about 13 kg/m 3 (22 lb/cu yd) (roughly 11 times heavier than air).
Tungsten tetrafluoride is an inorganic compound with the formula WF 4. This little studied solid has been invoked, together with tungsten pentafluoride , as an intermediate in the chemical vapor deposition of tungsten films using tungsten hexafluoride .
Tungsten(V) fluoride is an inorganic compound with the formula WF 5. It is a hygroscopic yellow solid. It is a hygroscopic yellow solid. Like most pentafluorides, it adopts a tetrameric structure, consisting of [WF 5 ] 4 molecules.
The reaction of tungsten(VI) oxytetrachloride and hydrogen fluoride will also produce WOF 4. [3] WOCl 4 + 4HF → WOF 4 + 4HCl. WOF 4 can also prepared by the reaction of lead(II) fluoride and tungsten trioxide at 700 °C. [3] 2PbF 2 + WO 3 → WOF 4 + 2PbO. Tungsten(VI) oxytetrafluoride hydrolyzes into tungstic acid. [1] [9] WOF 4 + 2 H 2 O ...
Tungsten fluoride may refer to: Tungsten tetrafluoride (tungsten(IV) fluoride) Tungsten pentafluoride (tungsten(V) fluoride) Tungsten hexafluoride (tungsten(VI) fluoride)
Tungsten(VI) oxide is soluble in aqueous base, forming tungstate (WO 4 2−). This oxyanion condenses at lower pH values, forming polyoxotungstates. [62] The broad range of oxidation states of tungsten is reflected in its various chlorides: [61] Tungsten(II) chloride, which exists as the hexamer W 6 Cl 12
Oxygen's highest fluoride is oxygen difluoride, [89] but fluorine can theoretically (as of 2012) oxidize it to a uniquely high oxidation state of +4 in the fluorocation: OF + 3. [90] In addition, several chalcogen fluorides occur which have more than one chalcogen (O 2 F 2, [91] S 2 F 10, [92] etc.).
Biotin and avidin bind with a dissociation constant of roughly 10 −15 M = 1 fM = 0.000001 nM. [7] Ribonuclease inhibitor proteins may also bind to ribonuclease with a similar 10 −15 M affinity. [8] The dissociation constant for a particular ligand–protein interaction can change with solution conditions (e.g., temperature, pH and