Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Gemma M. Locke"'
Autor:
Keith J. Flanagan, Maximilian Paradiz Dominguez, Zoi Melissari, Hans-Georg Eckhardt, René M. Williams, Dáire Gibbons, Caroline Prior, Gemma M. Locke, Alina Meindl, Aoife A. Ryan, Mathias O. Senge
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 17, Iss 1, Pp 1149-1170 (2021)
The use of halogens in the crystal engineering of supramolecular porphyrin assemblies has been a topic of strong interest over the past decades. With this in mind we have characterized a series of direct meso-halogenated porphyrins using single cryst
Externí odkaz:
https://doaj.org/article/966725d28ae5475d907f45398cd4c8dd
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 16, Iss 1, Pp 763-777 (2020)
Herein, 9,10-diethynyltriptycene is investigated for its use as a rigid isolating unit in the synthesis of multichromophoric arrays. Sonogashira cross-coupling conditions are utilized to attach various porphyrins and boron dipyrromethenes (BODIPYs) t
Externí odkaz:
https://doaj.org/article/c5b7340ac94e45338dca4b838a48f069
Publikováno v:
Beilstein Journal of Organic Chemistry
Beilstein Journal of Organic Chemistry, Vol 16, Iss 1, Pp 763-777 (2020)
Beilstein Journal of Organic Chemistry, Vol 16, Iss 1, Pp 763-777 (2020)
Herein, 9,10-diethynyltriptycene is investigated for its use as a rigid isolating unit in the synthesis of multichromophoric arrays. Sonogashira cross-coupling conditions are utilized to attach various porphyrins and boron dipyrromethenes (BODIPYs) t
Autor:
Michael H. R. Beh, Mathias O. Senge, Keith J. Flanagan, Nitika Grover, Gemma M. Locke, Alison Thompson
Publikováno v:
Chemistry (Weinheim an Der Bergstrasse, Germany)
Connecting two porphyrin units in a rigid linear fashion, without any undesired electron delocalization or communication between the chromophores, remains a synthetic challenge. Herein, a broad library of functionally diverse multi‐porphyrin arrays
Autor:
Aoife A. Ryan, Hans-Georg Eckhardt, Dáire Gibbons, Mathias O. Senge, Zoi Melissari, Caroline Prior, Gemma M. Locke, Keith J. Flanagan, Maximilian Paradiz Dominguez, René M. Williams, Alina Meindl
The use of halogens in the crystal engineering of porphyrin scaffolds has been a topic of strong interest over the past decades. Previously, this was focused on the introduction of a variety of halogens on the meso-phenyl groups of the porphyrin. How
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e33ec41ab1294ad86570e1eeb19fd3a
https://doi.org/10.3762/bxiv.2021.21.v1
https://doi.org/10.3762/bxiv.2021.21.v1
Autor:
Zoi Melissari, Mathias O. Senge, Dáire Gibbons, Keith J. Flanagan, Gemma M. Locke, Caroline Prior, Alina Meindl, Maximilian Paradiz Dominguez, Aoife A. Ryan, Hans-Georg Eckhardt, René M. Williams
Publikováno v:
Beilstein Journal of Organic Chemistry
Beilstein Journal of Organic Chemistry, Vol 17, Iss 1, Pp 1149-1170 (2021)
Beilstein Journal of Organic Chemistry, Vol 17, Iss 1, Pp 1149-1170 (2021)
The use of halogens in the crystal engineering of supramolecular porphyrin assemblies has been a topic of strong interest over the past decades. With this in mind we have characterized a series of direct meso-halogenated porphyrins using single cryst
Publikováno v:
Chemistry – A European Journal. 25
Autor:
Mathias O. Senge, Gemma M. Locke
Publikováno v:
ECS Transactions. 72:1-11
In nature, the antenna chlorophylls in photosynthetic bacteria are arranged as non-covalent macrorings in a spatially defined manner to absorb and transfer solar energy efficiently to the reaction centers. To mimic this, porphyrin assemblies with rig
Autor:
Keith J. Flanagan, Alison Thompson, Mathias O. Senge, Nitika Grover, Gemma M. Locke, Michael H. R. Beh
Publikováno v:
Chemistry – A European Journal. 26:2296-2296
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 25(18)
Nonconjugated hydrocarbons, like bicyclo[1.1.1]pentane, bicyclo[2.2.2]octane, triptycene, and cubane are a unique class of rigid linkers. Due to their similarity in size and shape they are useful mimics of classic benzene moieties in drugs, so-called