RT Journal Article
T1 Annulative π-extension of BODIPYs made easy via gold(i)-catalyzed cycloisomerization
A1 Labella, Jorge
A1 Durán Sampedro, Gonzalo
A1 Martínez-Díaz, María Victoria
A1 Torres, Tomás
AB Here we report gold(i)-catalyzed cycloisomerization as a new powerful synthetic tool for the preparation of pi-extended BODIPY derivatives. The catalytic system (PPh3AuCl)-Au-F/AgSbF(6)enables the synthesis of [b]-[2,1]naphtho-fused-BODIPYs (2a-2c) under mild conditions, in excellent yields and short reaction times. The reaction is totally regioselective to the 6-endo-dig product and for the alpha-position of the BODIPY, which is both the kinetically and thermodynamically favored pathway, as supported by the free energy profile calculated by means of Density Functional Theory (DFT). Moreover, this methodology also allows the synthesis of two new families of [b]-aryl-fused-BODIPYs, namely, [3,4]phenanthro- (2eand2f) and [1,2]naphtho-fused (2g) BODIPYs. Their molecular and electronic structures were established by NMR and UV-vis spectroscopies as well as single-crystal X-ray diffraction analysis. As can be noted from the X-ray structures,2a,2eand2gpresent interesting structural differences at both the molecular and packing level. Interestingly, despite being isomers, the UV/vis spectra of2aand2grevealed significant differences in their electronic structures. The origin of this finding was studied by Time-Dependent DFT calculations. Calculated DFT Nuclear Independent Chemical Shift (NICS(0)) values also supported the different electronic structures of2aand2g.
PB Royal Society of Chemistry
SN 2041-6520
YR 2020
FD 2020
LK https://hdl.handle.net/20.500.14352/95509
UL https://hdl.handle.net/20.500.14352/95509
LA eng
NO Labella, Jorge, et al. «Annulative π-Extension of BODIPYs Made Easy via Gold( i )-Catalyzed Cycloisomerization». Chemical Science, vol. 11, n.o 39, 2020, pp. 10778-85.  https://doi.org/10.1039/D0SC01054E.
NO Ministerio de Economia y Competitividad (España)
NO European Commission
DS Docta Complutense
RD 10 abr 2025