Abstract

Many attempts have been made in order to realize organic ferromagnetic materials. Triplet carbenes are regarded as one of the most effective spin sources since magnitude of the exchange coupling between the neighboring centers is large. However, those systems have not employed extensively due to two disadvantages that hinder their further extension to usable magnetic materials. First, a triplet carbene unit is highly unstable and lacks the stability for practical application under ambient conditions. In order to overcome these difficulties, we have made great efforts to stabilize and succeeded in preparing fairly stable ones surviving for days. The second disadvantage that arises is that diazo groups are also generally labile and, hence, are usually introduced at the last step of synthesis.We found, more or less by chance, that a diphenyldiazomethane for a persistent triplet carbene is also persistent at the stage of the diazo compound and, hence, can be further modified, with the diazo group intact, into a more complicated diazo compound. Thus, the diazo compound can be used as a building block to prepare a poly (diazo) compound, which can then generate high-spin polycarbene with considerable thermal stability. Here we would like to summarize how we have used this method to prepare a series of poly (diazo) compounds. Attempts to modify the diazo compound to a more congested derivative by taking advantage of the stability are also mentioned.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.