Subphthalocyanine capsules: molecular reactors for photoredox transformations of fullerenes

Marta Moreno-Simoni; Tomas Torres; Gema de la Torre

doi:10.1039/d2sc01931k

journal article Open Access Jan 01, 2022

Subphthalocyanine capsules: molecular reactors for photoredox transformations of fullerenes

Marta Moreno-Simoni Tomas Torres

Gema de la Torre

Chemical Science Vol. 13 No. 32 pp. 9249-9255 · Royal Society of Chemistry (RSC)

View at Publisher Save 10.1039/d2sc01931k

Abstract

A photoredox cage built by coordination of two pyridyl-subphthalocyanines to Pd centers has proved versatile and efficient to catalyze photoredox addition reactions over encapsulated C60.

Topics

No keywords indexed for this article. Browse by subject →

References

47

[1]

Brown Chem. Rev. (2015) 10.1021/cr4001226

[2]

Xue Coord. Chem. Rev. (2021) 10.1016/j.ccr.2020.213656

[3]

C. R. J.Stephenson , T. P.Yoon and D. W. C.MacMillan , Visible Light Photocatalysis in Organic Chemistry , Wiley-VCH , Weinheim, Germany 2018 10.1002/9783527674145

[4]

T.Comerford , E.Zysman-Colman and M. D.Ward , in Reactivity in Confined Spaces , ed., R. S. Forgan and G. O Lloyd , The Royal Society of Chemistry , 2021 , pp. 70–107 10.1039/9781788019705-00070

[5]

Lin Chem.–Asian J. (2021) 10.1002/asia.202100942

[6]

Visible Light Photoredox Catalysis with Transition Metal Complexes: Applications in Organic Synthesis

Christopher K. Prier, Danica A. Rankic, David W. C. MacMillan

Chemical Reviews 2013 10.1021/cr300503r

[7]

Organic Photoredox Catalysis

Nathan A. Romero, David A. Nicewicz

Chemical Reviews 2016 10.1021/acs.chemrev.6b00057

[8]

Bottari Coord. Chem. Rev. (2021) 10.1016/j.ccr.2020.213605

[9]

Claessens Chem. Rev. (2014) 10.1021/cr400088w

[10]

de la Torre Adv. Energy Mater. (2017) 10.1002/aenm.201601700

[11]

Zango Chem. Sci. (2020) 10.1039/d0sc00059k

[12]

Claessens J. Am. Chem. Soc. (2002) 10.1021/ja028705j

[13]

Claessens Chem. Commun. (2004) 10.1039/b401232a

[14]

Sánchez-Molina J. Am. Chem. Soc. (2013) 10.1021/ja404234n

[15]

Ronson J. Am. Chem. Soc. (2016) 10.1021/jacs.6b06710

[16]

Han Chem. Commun. (2018) 10.1039/c8cc06652c

[17]

Fazio Chem. Commun. (2018) 10.1039/c7cc09528g

[18]

García-Simón Chem. Commun. (2019) 10.1039/c8cc07886f

[19]

Chen J. Am. Chem. Soc. (2019) 10.1021/jacs.9b02207

[20]

Barendt J. Am. Chem. Soc. (2020) 10.1021/jacs.9b10929

[21]

Chang J. Am. Chem. Soc. (2020) 10.1021/jacs.0c06623

[22]

Ni J. Am. Chem. Soc. (2020) 10.1021/jacs.0c04876

[23]

Fuertes-Espinosa Chem.– Eur. J. (2017) 10.1002/chem.201700046

[24]

Martínez-Agramunt Angew. Chem., Int. Ed. (2019) 10.1002/anie.201901586

[25]

Wood Angew. Chem., Int. Ed. (2015) 10.1002/anie.201411985

[26]

Leonhardt Chem. Sci. (2020) 10.1039/d0sc03131c

[27]

Fuertes-Espinosa Chem (2020) 10.1016/j.chempr.2019.10.010

[28]

Ubasart Nat. Chem. (2021) 10.1038/s41557-021-00658-6

[29]

Huang J. Am. Chem. Soc. (2018) 10.1021/jacs.8b02710

[30]

Castro J. Mater. Chem. B (2017) 10.1039/c7tb00855d

[31]

Katsurayama Chem.– Eur. J. (2022) 10.1002/chem.202103223

[32]

Ishikawa Chem. Commun. (2021) 10.1039/d1cc06307c

[33]

Matsuzaki ChemistryOpen (2017) 10.1002/open.201600172

[34]

Tzirakis Chem. Rev. (2013) 10.1021/cr300475r

[35]

Nakamura J. Org. Chem. (2005) 10.1021/jo051253j

[36]

Jeong Org. Biomol. Chem. (2016) 10.1039/c6ob02069k

[37]

Lim Tetrahedron Lett. (2015) 10.1016/j.tetlet.2014.10.060

[38]

Lim J. Org. Chem. (2014) 10.1021/jo501034t

[39]

Jeong Tetrahedron Lett. (2017) 10.1016/j.tetlet.2017.01.073

[40]

Miyake Chem.– Eur. J. (2014) 10.1002/chem.201304731

[41]

Kim ACS Catal. (2020) 10.1021/acscatal.0c02443

[42]

Tzirakis Chem. Rev. (2013) 10.1021/cr300475r

[43]

Rosso Org. Lett. (2019) 10.1021/acs.orglett.9b01992

[44]

Sumino J. Org. Chem. (2017) 10.1021/acs.joc.7b00609

[45]

Morton J. Phys. Chem. (1995) 10.1021/j100025a011

[46]

Kostromitin Chem. Commun. (2021) 10.1039/d1cc01609a

[47]

Xu Chem. Commun. (2018) 10.1039/c8cc06019c

Metrics

21

Citations

47

References

Details

Published: Jan 01, 2022
Vol/Issue: 13(32)
Pages: 9249-9255
License: View

Authors

M

Marta Moreno-Simoni

Organic Chemistry Department, Universidad Autónoma de Madrid, Campus de Cantoblanco, 28049-Madrid, Spain

T

Tomas Torres

Organic Chemistry Department, Universidad Autónoma de Madrid, Campus de Cantoblanco, 28049-Madrid, Spain; Institute for Advanced Research in Chemical Sciences (IAdChem), Universidad Autónoma de Madrid, Campus de Cantoblanco, 28049-Madrid, Spain; IMDEA-Nanociencia, C/Faraday 9, 28049-Madrid, Spain

G

Gema de la Torre

Organic Chemistry Department, Universidad Autónoma de Madrid, Campus de Cantoblanco, 28049-Madrid, Spain; Institute for Advanced Research in Chemical Sciences (IAdChem), Universidad Autónoma de Madrid, Campus de Cantoblanco, 28049-Madrid, Spain

Cite This Article

Marta Moreno-Simoni, Tomas Torres, Gema de la Torre (2022). Subphthalocyanine capsules: molecular reactors for photoredox transformations of fullerenes. Chemical Science, 13(32), 9249-9255. https://doi.org/10.1039/d2sc01931k

Subphthalocyanine capsules: molecular reactors for photoredox transformations of fullerenes

You May Also Like