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Sung, Young Mo,Szyszko, Bartosz,Myx15b,liborski, Radomir,Stx119,piex144,, Marcin,Oh, Juwon,Son, Minjung,Latos-Graż,yx144,ski, Lechosław,Kim, Dongho The Royal Society of Chemistry 2014 Chemical communications Vol.50 No.61
<P>In a series of thiaaceneporphyrinoids, their conformers exhibit macrocyclic π-conjugation pathways controlled by a dihedral angle between the porphyrin framework and acene planes. Conformational equilibria significantly affect the photophysical properties of these macrocycles.</P> <P>Graphic Abstract</P><P>In a series of thiaaceneporphyrinoids, their conformers exhibit macrocyclic π-conjugation pathways controlled by a dihedral angle between the porphyrin framework and acene planes. <IMG SRC='http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=c4cc03855j'> </P>