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CsF is more soluble than sodium fluoride or potassium fluoride in organic solvents. It is available in its anhydrous form, and if water has been absorbed, it is easy to dry by heating at 100 °C for two hours in vacuo. [7] CsF reaches a vapor pressure of 1 kilopascal at 825 °C, 10 kPa at 999 °C, and 100 kPa at 1249 °C. [8]
In inorganic chemistry, Fajans' rules, formulated by Kazimierz Fajans in 1923, [1] [2] [3] are used to predict whether a chemical bond will be covalent or ionic, and depend on the charge on the cation and the relative sizes of the cation and anion. They can be summarized in the following table:
Reference ranges for other CSF constituents Substance Lower limit Upper limit Unit Corresponds to % of that in blood plasma; RBCs: n/a [2] 0 [2] / negative: cells/μL or
In the crystal (CsF has the NaCl structure with both ions being 6-coordinate) if each bond has 9% covalent character the total covalency of Cs and F would be 54%. This would be represented by one bond of around 50% covalent character resonating between the six positions and the overall effect would be to reduce the charge on Cs to about + 0.5 ...
Cerebrospinal fluid (CSF) is a clear, colorless body fluid found within the tissue that surrounds the brain and spinal cord of all vertebrates. CSF is produced by specialized ependymal cells in the choroid plexus of the ventricles of the brain, and absorbed in the arachnoid granulations. In humans, there is about 125 mL of CSF at any one time ...
The covalent radius of fluorine of about 71 picometers found in F 2 molecules is significantly larger than that in other compounds because of this weak bonding between the two fluorine atoms. [9] This is a result of the relatively large electron and internuclear repulsions, combined with a relatively small overlap of bonding orbitals arising ...
The carbon–fluorine bond is a polar covalent bond between carbon and fluorine that is a component of all organofluorine compounds. It is one of the strongest single bonds in chemistry (after the B–F single bond, Si–F single bond, and H–F single bond), and relatively short, due to its partial ionic character.
Others point to the ionic nature of the bonds in BF 3. [8] Synthesis and handling ... CsF + BF 3 → Cs[BF 4] O(CH 2 CH 3) 2 + BF 3 → BF 3 ·O ...