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S-Nitrosotriphenylmethanethiol is the organosulfur compound with the formula (C6H5)3CSNO. It is a rare example of a nitrosothiol derivative that is robust solid at room temperature. The green compound can be produced by the reaction of triphenylmethanethiol with nitrous acid: (C6H5)3CSH + HONO → (C6H5)3CSNO + H2O

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  • S-Nitrosotriphenylmethanethiol (en)
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  • S-Nitrosotriphenylmethanethiol is the organosulfur compound with the formula (C6H5)3CSNO. It is a rare example of a nitrosothiol derivative that is robust solid at room temperature. The green compound can be produced by the reaction of triphenylmethanethiol with nitrous acid: (C6H5)3CSH + HONO → (C6H5)3CSNO + H2O (en)
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  • S-Nitrosotriphenylmethanethiol (en)
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  • S-Nitrosotriphenylmethanethiol (en)
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  • http://commons.wikimedia.org/wiki/Special:FilePath/Ph3CSNO.svg
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  • Ph3CSNO.svg (en)
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  • S-Nitrosotriphenylmethanethiol is the organosulfur compound with the formula (C6H5)3CSNO. It is a rare example of a nitrosothiol derivative that is robust solid at room temperature. The green compound can be produced by the reaction of triphenylmethanethiol with nitrous acid: (C6H5)3CSH + HONO → (C6H5)3CSNO + H2O According to X-ray crystallography, S-nitrosotriphenylmethanethiol features a conventional trityl group appended to a bent SNO substituent. The S-N=O angle is 114°, while the S-N and N=O distances are 1.78 and 1.79 Å. Other S-nitrosothiols, e.g. MeSNO and SNAP have characterized by similar structures. (en)
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