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The photochemistry of 9-diazo-l,8-diazafluorene (18DAF) depends on the wavelength of the irradiating light. When photolyzed at ca. 310 nm, into a -* absorption band, excited 18DAF rearranges to a diazirine and loses nitrogen to form the carbene 1,8-diazafluorenylidene (18FL) exclusively in the singlet state. However, when 18DAF is photolyzed at ca. 420 nm, into the -* band, no diazirine is formed, but triplet 18FL is formed directly along (4) Turro, N.
The photochemistry of 9-diazo-l,8-diazafluorene (18DAF) depends on the wavelength of the irradiating light. When photolyzed at ca. 310 nm, into a -* absorption band, excited 18DAF rearranges to a diazirine and loses nitrogen to form the carbene 1,8-diazafluorenylidene (18FL) exclusively in the singlet state. However, when 18DAF is photolyzed at ca. 420 nm, into the -* band, no diazirine is formed, but triplet 18FL is formed directly along (4) Turro, N.
The article contains sections titled: 1. Introduction 2. Nitration 2.1. Nitrating Agents 2.2. Reaction Mechanisms 3. Nitro Aromatics 3.1. Nitrobenzenes 3.2. Nitrotoluenes 3.3. Nitroxylenes 3.4. Nitronaphthalenes 3.5. Other Nitro Aromatics 4. Nitrohalo Aromatics 4.1. Chloronitrobenzenes 4.2. Dichloro‐ and Polychloronitrobenzenes 4.3. Chloronitrotoluenes 4.4. Fluoronitrobenzenes and Fluoronitrotoluenes 5. Nitroamino Aromatics 5.1. Nitroanilines 5.2. Nitrotoluidines 5.3. Halogenonitroanilines 5.4. Cyanonitroanilines 6. Nitroaromatic Sulfonic Acids and Derivatives 6.1. Nitrobenzenesulfonic acids and Derivatives 6.2. Nitrotoluenesulfonic Acids and Derivatives 6.3. Chloronitrobenzenesulfonic Acids and Derivatives 6.4. Chloronitrotoluenesulfonic Acids 7. Nitrohydroxy and Alkoxy Aromatics 7.1. Nitrophenols and Derived Ethers 7.2. Nitroalkylphenols 8. Nitroketones 9. Nitroheterocycles 9.1. Pyridine Derivatives 9.2. Quinoline Derivatives 9.3. Imidazole Derivatives 9.4. Furan Derivatives 9.5. Thiophene Derivatives 9.6. Thiazole Derivatives
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