Template-controlled on-surface synthesis of a lanthanide supernaphthalocyanine and its open-chain polycyanine counterpart

Extending the π‐conjugation of phthalocyanine dyes, while synthetically challenging, has the potential to produce desirable new molecular materials. Here, the authors use a templated on‐surface approach to synthesize several extended phthalocyanine derivatives from the same building block, including...

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Autores principales:	Qitang Fan, Jan-Niclas Luy, Martin Liebold, Katharina Greulich, Malte Zugermeier, Jörg Sundermeyer, Ralf Tonner, J. Michael Gottfried
Formato:	article
Lenguaje:	EN
Publicado:	Nature Portfolio 2019
Materias:	Science Q
Acceso en línea:	https://doaj.org/article/ce5bc62cf9cf4c9792f54acc8409dcbc
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spelling	oai:doaj.org-article:ce5bc62cf9cf4c9792f54acc8409dcbc2021-12-02T15:36:24ZTemplate-controlled on-surface synthesis of a lanthanide supernaphthalocyanine and its open-chain polycyanine counterpart10.1038/s41467-019-13030-72041-1723https://doaj.org/article/ce5bc62cf9cf4c9792f54acc8409dcbc2019-11-01T00:00:00Zhttps://doi.org/10.1038/s41467-019-13030-7https://doaj.org/toc/2041-1723Extending the π‐conjugation of phthalocyanine dyes, while synthetically challenging, has the potential to produce desirable new molecular materials. Here, the authors use a templated on‐surface approach to synthesize several extended phthalocyanine derivatives from the same building block, including a lanthanide superphthalocyanine and an open‐chain polycyanine.Qitang FanJan-Niclas LuyMartin LieboldKatharina GreulichMalte ZugermeierJörg SundermeyerRalf TonnerJ. Michael GottfriedNature PortfolioarticleScienceQENNature Communications, Vol 10, Iss 1, Pp 1-8 (2019)
institution	DOAJ
collection	DOAJ
language	EN
topic	Science Q
spellingShingle	Science Q Qitang Fan Jan-Niclas Luy Martin Liebold Katharina Greulich Malte Zugermeier Jörg Sundermeyer Ralf Tonner J. Michael Gottfried Template-controlled on-surface synthesis of a lanthanide supernaphthalocyanine and its open-chain polycyanine counterpart
description	Extending the π‐conjugation of phthalocyanine dyes, while synthetically challenging, has the potential to produce desirable new molecular materials. Here, the authors use a templated on‐surface approach to synthesize several extended phthalocyanine derivatives from the same building block, including a lanthanide superphthalocyanine and an open‐chain polycyanine.
format	article
author	Qitang Fan Jan-Niclas Luy Martin Liebold Katharina Greulich Malte Zugermeier Jörg Sundermeyer Ralf Tonner J. Michael Gottfried
author_facet	Qitang Fan Jan-Niclas Luy Martin Liebold Katharina Greulich Malte Zugermeier Jörg Sundermeyer Ralf Tonner J. Michael Gottfried
author_sort	Qitang Fan
title	Template-controlled on-surface synthesis of a lanthanide supernaphthalocyanine and its open-chain polycyanine counterpart
title_short	Template-controlled on-surface synthesis of a lanthanide supernaphthalocyanine and its open-chain polycyanine counterpart
title_full	Template-controlled on-surface synthesis of a lanthanide supernaphthalocyanine and its open-chain polycyanine counterpart
title_fullStr	Template-controlled on-surface synthesis of a lanthanide supernaphthalocyanine and its open-chain polycyanine counterpart
title_full_unstemmed	Template-controlled on-surface synthesis of a lanthanide supernaphthalocyanine and its open-chain polycyanine counterpart
title_sort	template-controlled on-surface synthesis of a lanthanide supernaphthalocyanine and its open-chain polycyanine counterpart
publisher	Nature Portfolio
publishDate	2019
url	https://doaj.org/article/ce5bc62cf9cf4c9792f54acc8409dcbc
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Template-controlled on-surface synthesis of a lanthanide supernaphthalocyanine and its open-chain polycyanine counterpart

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