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Part 1: Document Description
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Citation |
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Title: |
A Series of Soluble Thieno-fused Coronene Nanoribbons of Precise Lengths [Data] |
Identification Number: |
doi:10.11588/data/30AOAT |
Distributor: |
heiDATA |
Date of Distribution: |
2022-11-23 |
Version: |
1 |
Bibliographic Citation: |
Yang, Xuan; Elbert, Sven Michael; Rominger, Frank; Mastalerz, Michael, 2022, "A Series of Soluble Thieno-fused Coronene Nanoribbons of Precise Lengths [Data]", https://doi.org/10.11588/data/30AOAT, heiDATA, V1 |
Citation |
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Title: |
A Series of Soluble Thieno-fused Coronene Nanoribbons of Precise Lengths [Data] |
Identification Number: |
doi:10.11588/data/30AOAT |
Authoring Entity: |
Yang, Xuan (Institute of Organic Chemistry, Heidelberg University) |
Elbert, Sven Michael (Institute of Organic Chemistry, Heidelberg University) |
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Rominger, Frank (Institute of Organic Chemistry, Heidelberg University) |
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Mastalerz, Michael (Institute of Organic Chemistry, Heidelberg University) |
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Grant Number: |
SFB 1249 (TP-A04) |
Distributor: |
heiDATA |
Access Authority: |
Mastalerz, Michael |
Depositor: |
Schwesinger, Georg Gustav |
Date of Deposit: |
2022-03-09 |
Holdings Information: |
https://doi.org/10.11588/data/30AOAT |
Study Scope |
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Keywords: |
Chemistry, Absorption, Aromatic Compounds, Hydrocarbons, Precursors, Two Dimensional Materials |
Abstract: |
Among graphene nanoribbons (GNRs), reports on coronene-based GNRs were very rare, despite the unique optoelectronic properties of coronene. Herein, the synthesis of a series of structurally precise and soluble thieno-fused coronene nanoribbons (CR-1 to CR-4) with up to four coronene units connected through benzene rings along their K-regions is described by two different synthetic approaches. Due to the triptycene end-caps all CRs are highly soluble, allowing to characterize such structures in solution and study the length dependent photophysical properties which are supported by theoretical calculations. |
Methodology and Processing |
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Data Access |
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Other Study Description Materials |
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Related Publications |
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Citation |
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Title: |
J. Am. Chem. Soc. 2022, 144, 22, 9883–9892 |
Identification Number: |
10.1021/jacs.2c02645 |
Bibliographic Citation: |
J. Am. Chem. Soc. 2022, 144, 22, 9883–9892 |
Label: |
Compound 10_Triptycene Monoboronic Ester_XY730.zip |
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application/zip |
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Compound 11_PO-5-2Thio-precursor_XY747.zip |
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application/zip |
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Compound 12_PO-9-4Thio-precursor_XY734.zip |
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application/zip |
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Compound 13_Triptycene Monobromide_XY733.zip |
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application/zip |
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Compound 14_PO-13-6Thio-precursor_XY738.zip |
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application/zip |
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Compound 15_Diboronic Ester_XY735.zip |
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Compound 16_PO-17-8Thio-precursor_XY739.zip |
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application/zip |
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Compound 17_PO-17-8Thio_XY742.zip |
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application/zip |
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Compound 1_PO-5-2Br_XY422.zip |
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application/zip |
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Compound 2_PO-9-4Br_XY531 XY667.zip |
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application/zip |
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Compound 3_PO-13-6Br_XY672.zip |
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Compound 4_PO-5-2Thio_XY665.zip |
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Compound 5_PO-9-4Thio_XY670.zip |
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Compound 6_PO-13-6Thio_XY741.zip |
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Compound 7_Triptycene Monoketone_XY729.zip |
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application/zip |
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Compound 9_Dibromodiketone_XY700 XY732.zip |
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application/zip |
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Compound S1_Thiophene Aldehyde_XY728.zip |
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application/zip |
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CR-1_XY669.zip |
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application/zip |
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CR-2_XY673.zip |
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application/zip |
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CR-3_XY743.zip |
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application/zip |
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CR-4_XY744.zip |
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application/zip |