RESUMO
The cyclobutane cleavage reaction is an important process and has received continuous interest. Herein, we demonstrate the visible laser-driven cleavage reaction of cyclobutane in crystal form by using inâ situ Raman spectroscopy. Silver(I) coordination-induced strain and thermal effects from the laser irradiation are the two main driving forces for the cleavage of cyclobutane crystals. This work may open up a new avenue for studying cyclobutane cleavage reactions, as compared to the conventional routes using exâ situ techniques.
Assuntos
Ciclobutanos/química , Prata/química , Ciclobutanos/efeitos da radiação , Luz , Compostos Organometálicos/química , Análise Espectral Raman , Ácido Trifluoracético/químicaRESUMO
The Sn atom of the title compound, [Sn(C(2)H(5))(2)(C(12)H(12)BrNO(3))], is in a distorted SnNC(2)O(2) trigonal-bipyramidal geometry and forms five- and six-membered chelate rings with the tridentate ligand. One C atom of one ethyl group is disordered with site occupancies of 0.61â (3):0.39â (3).
RESUMO
Visible laser induced [2+2] cycloaddition of solid-state pyridine substituted olefins into cyclobutane has been monitored by an in situ Raman technique. The laser power and wavelength can dramatically alter the reaction kinetics, as a prior melting process (heating from laser irradiation) is required for this [2+2] photoreaction.