2026-07-11T23:04:58Zhttp://localhost:3000{"from"=>"2022-08-01T14:15:00Z", "until"=>"2022-09-01T14:20:00Z", "metadataPrefix"=>"oai_datacite", "verb"=>"ListRecords"}

10.14272/FERUHHWVLZNKMW-UHFFFAOYSA-N/CHMO0000595.22022-08-11T20:02:11Zpublicationpublication:datasets

4.4TIB.KIT-IOC https://dx.doi.org/10.14272/FERUHHWVLZNKMW-UHFFFAOYSA-N/CHMO0000595.2 Krämer, Joana Joana Krämer 0000-0003-0498-7298 Institute of Nanotechnology (INT), Karlsruhe Institute of Technology, Germany chemotion.net 2022 Krämer, Joana Joana Krämer 0000-0003-0498-7298 Institute of Nanotechnology (INT), Karlsruhe Institute of Technology, Germany 2022-07-03 09:44:12 UTC 2022-08-11 20:01:58 UTC Chemistry en Dataset 1 Attribution-ShareAlike 4.0 International (CC BY-SA 4.0) dataset for 13C nuclear magnetic resonance spectroscopy (13C NMR)
13C NMR (126 Hz, chloroform-d1, ppm) δ = 163.3 (4Cq), 131.2 (4Cq), 126.8 (2Cq), 126.8 (4CH), 27.6 (2CH3). https://dx.doi.org/10.14272/FERUHHWVLZNKMW-UHFFFAOYSA-N.3

10.14272/FERUHHWVLZNKMW-UHFFFAOYSA-N.32022-08-11T20:02:11Zpublicationpublication:samples

4.4TIB.KIT-IOC https://dx.doi.org/10.14272/FERUHHWVLZNKMW-UHFFFAOYSA-N.3 Krämer, Joana Joana Krämer 0000-0003-0498-7298 Institute of Nanotechnology (INT), Karlsruhe Institute of Technology, Germany chemotion.net 2022 Krämer, Joana Joana Krämer 0000-0003-0498-7298 Institute of Nanotechnology (INT), Karlsruhe Institute of Technology, Germany 2022-07-03 09:44:12 UTC 2022-08-11 20:01:58 UTC Chemistry en Molecule 1 This dataset contains experimental data from a sample (6,13-dimethyl-6,13-diazatetracyclo[6.6.2.04,16.011,15]hexadeca-1(15),2,4(16),8,10-pentaene-5,7,12,14-tetrone, InChI=1S/C16H10N2O4/c1-17-13(19)7-3-5-9-12-10(16(22)18(2)15(9)21)6-4-8(11(7)12)14(17)20/h3-6H,1-2H3).
The datasets from the following experiments are available:
1H nuclear magnetic resonance spectroscopy (1H NMR)
13C nuclear magnetic resonance spectroscopy (13C NMR)
https://dx.doi.org/10.14272/FERUHHWVLZNKMW-UHFFFAOYSA-N/CHMO0000593.2 https://dx.doi.org/10.14272/FERUHHWVLZNKMW-UHFFFAOYSA-N/CHMO0000595.2 https://dx.doi.org/10.14272/reaction/SA-FUHFF-UHFFFADPSC-FERUHHWVLZ-UHFFFADPSC-NUHFF-NUHFF-NUHFF-ZZZ.1

10.14272/FERUHHWVLZNKMW-UHFFFAOYSA-N/CHMO0000593.22022-08-11T20:02:11Zpublicationpublication:datasets

4.4TIB.KIT-IOC https://dx.doi.org/10.14272/FERUHHWVLZNKMW-UHFFFAOYSA-N/CHMO0000593.2 Krämer, Joana Joana Krämer 0000-0003-0498-7298 Institute of Nanotechnology (INT), Karlsruhe Institute of Technology, Germany chemotion.net 2022 Krämer, Joana Joana Krämer 0000-0003-0498-7298 Institute of Nanotechnology (INT), Karlsruhe Institute of Technology, Germany 2022-07-03 09:44:12 UTC 2022-08-11 20:01:58 UTC Chemistry en Dataset 1 Attribution-ShareAlike 4.0 International (CC BY-SA 4.0) dataset for 1H nuclear magnetic resonance spectroscopy (1H NMR)
1H NMR (500 MHz, chloroform-d1, ppm) δ = 8.78 (s, 4H, H-Ar), 3.61 (s, 6H, CH3). https://dx.doi.org/10.14272/FERUHHWVLZNKMW-UHFFFAOYSA-N.3

10.14272/reaction/SA-FUHFF-UHFFFADPSC-FERUHHWVLZ-UHFFFADPSC-NUHFF-NUHFF-NUHFF-ZZZ.12022-08-11T20:02:10Zpublicationpublication:reactions

4.4TIB.KIT-IOC https://dx.doi.org/10.14272/reaction/SA-FUHFF-UHFFFADPSC-FERUHHWVLZ-UHFFFADPSC-NUHFF-NUHFF-NUHFF-ZZZ.1 Krämer, Joana Joana Krämer 0000-0003-0498-7298 Institute of Nanotechnology (INT), Karlsruhe Institute of Technology, Germany chemotion.net 2022 Krämer, Joana Joana Krämer 0000-0003-0498-7298 Institute of Nanotechnology (INT), Karlsruhe Institute of Technology, Germany 2022-07-03 09:44:11 UTC 2022-08-11 20:01:58 UTC chemical reaction: structures conditions en reaction conditions 1 Attribution-ShareAlike 4.0 International (CC BY-SA 4.0) A three-neck flask equipped with a reflux condenser was filled with 120 mL aqueous methylamine (40.0 wt%, 1.39 mol, 74.6 eq) and 5.00 g of 1,4,5,8‑naphtalenetetracarboxylic dianhydride (18.6 mmol, 1.00 eq) were slowly added under vigorous stirring. The orange-brown solution was refluxed at 100 °C for 3 h, cooled down to 25 °C and stirred for 2 days. The formed precipitate was collected by filtration, washed with 100 mL of methanol and dried in vacuo. The product was isolated as a nude-coloured solid with a yield of 56 % (3.09 g, 10.5 mmol). https://dx.doi.org/10.14272/FERUHHWVLZNKMW-UHFFFAOYSA-N.3 https://dx.doi.org/10.1021/ja00128a015

10.14272/JMHFTDFPRQWUAN-UHFFFAOYSA-H.192022-08-10T07:16:45Zpublicationpublication:samples

4.4TIB.KIT-IOC https://dx.doi.org/10.14272/JMHFTDFPRQWUAN-UHFFFAOYSA-H.19 Pilz, Lena Lena Pilz 0000-0002-5616-9003 Institute of Functional Interfaces, Karlsruhe Institute of Technology, Deutschland chemotion.net 2022 Pilz, Lena Lena Pilz 0000-0002-5616-9003 Institute of Functional Interfaces, Karlsruhe Institute of Technology, Deutschland 2022-07-28 09:28:52 UTC 2022-08-05 15:26:28 UTC Chemistry en Molecule 1 This dataset contains experimental data from a sample (dicopper;benzene-1,3,5-tricarboxylate, InChI=1S/2C9H6O6.2Cu/c2*10-7(11)4-1-5(8(12)13)3-6(2-4)9(14)15;;/h2*1-3H,(H,10,11)(H,12,13)(H,14,15);;/q;;2*+2/p-6).
The datasets from the following experiments are available:
X-ray diffraction (XRD)
X-ray diffraction (XRD)
single crystal X-ray diffraction (single-crystal X-ray diffraction)
https://dx.doi.org/10.14272/JMHFTDFPRQWUAN-UHFFFAOYSA-H/CHMO0000156.35 https://dx.doi.org/10.14272/JMHFTDFPRQWUAN-UHFFFAOYSA-H/CHMO0000159.17 https://dx.doi.org/10.14272/JMHFTDFPRQWUAN-UHFFFAOYSA-H/CHMO0000156.36 https://dx.doi.org/10.14272/reaction/SA-FUHFF-UHFFFADPSC-JMHFTDFPRQ-UHFFFADPSC-NUHFF-HUHFF-NUHFF-ZZZ.18

10.14272/JMHFTDFPRQWUAN-UHFFFAOYSA-H.152022-08-10T07:16:45Zpublicationpublication:samples

4.4TIB.KIT-IOC https://dx.doi.org/10.14272/JMHFTDFPRQWUAN-UHFFFAOYSA-H.15 Pilz, Lena Lena Pilz 0000-0002-5616-9003 Institute of Functional Interfaces, Karlsruhe Institute of Technology, Deutschland chemotion.net 2022 Pilz, Lena Lena Pilz 0000-0002-5616-9003 Institute of Functional Interfaces, Karlsruhe Institute of Technology, Deutschland 2022-07-28 09:27:36 UTC 2022-08-05 15:16:55 UTC Chemistry en Molecule 1 This dataset contains experimental data from a sample (dicopper;benzene-1,3,5-tricarboxylate, InChI=1S/2C9H6O6.2Cu/c2*10-7(11)4-1-5(8(12)13)3-6(2-4)9(14)15;;/h2*1-3H,(H,10,11)(H,12,13)(H,14,15);;/q;;2*+2/p-6).
The datasets from the following experiments are available:
X-ray diffraction (XRD)
X-ray diffraction (XRD)
single crystal X-ray diffraction (single-crystal X-ray diffraction)
https://dx.doi.org/10.14272/JMHFTDFPRQWUAN-UHFFFAOYSA-H/CHMO0000156.28 https://dx.doi.org/10.14272/JMHFTDFPRQWUAN-UHFFFAOYSA-H/CHMO0000156.27 https://dx.doi.org/10.14272/JMHFTDFPRQWUAN-UHFFFAOYSA-H/CHMO0000159.13 https://dx.doi.org/10.14272/reaction/SA-FUHFF-UHFFFADPSC-JMHFTDFPRQ-UHFFFADPSC-NUHFF-HUHFF-NUHFF-ZZZ.14

10.14272/JMHFTDFPRQWUAN-UHFFFAOYSA-H.132022-08-10T07:16:45Zpublicationpublication:samples

4.4TIB.KIT-IOC https://dx.doi.org/10.14272/JMHFTDFPRQWUAN-UHFFFAOYSA-H.13 Pilz, Lena Lena Pilz 0000-0002-5616-9003 Institute of Functional Interfaces, Karlsruhe Institute of Technology, Deutschland chemotion.net 2022 Pilz, Lena Lena Pilz 0000-0002-5616-9003 Institute of Functional Interfaces, Karlsruhe Institute of Technology, Deutschland 2022-07-28 09:26:57 UTC 2022-08-05 15:12:21 UTC Chemistry en Molecule 1 This dataset contains experimental data from a sample (dicopper;benzene-1,3,5-tricarboxylate, InChI=1S/2C9H6O6.2Cu/c2*10-7(11)4-1-5(8(12)13)3-6(2-4)9(14)15;;/h2*1-3H,(H,10,11)(H,12,13)(H,14,15);;/q;;2*+2/p-6).
The datasets from the following experiments are available:
X-ray diffraction (XRD)
X-ray diffraction (XRD)
single crystal X-ray diffraction (single-crystal X-ray diffraction)
https://dx.doi.org/10.14272/JMHFTDFPRQWUAN-UHFFFAOYSA-H/CHMO0000156.24 https://dx.doi.org/10.14272/JMHFTDFPRQWUAN-UHFFFAOYSA-H/CHMO0000156.23 https://dx.doi.org/10.14272/JMHFTDFPRQWUAN-UHFFFAOYSA-H/CHMO0000159.11 https://dx.doi.org/10.14272/reaction/SA-FUHFF-UHFFFADPSC-JMHFTDFPRQ-UHFFFADPSC-NUHFF-HUHFF-NUHFF-ZZZ.12

10.14272/JMHFTDFPRQWUAN-UHFFFAOYSA-H.182022-08-10T07:16:45Zpublicationpublication:samples

4.4TIB.KIT-IOC https://dx.doi.org/10.14272/JMHFTDFPRQWUAN-UHFFFAOYSA-H.18 Pilz, Lena Lena Pilz 0000-0002-5616-9003 Institute of Functional Interfaces, Karlsruhe Institute of Technology, Deutschland chemotion.net 2022 Pilz, Lena Lena Pilz 0000-0002-5616-9003 Institute of Functional Interfaces, Karlsruhe Institute of Technology, Deutschland 2022-07-28 09:28:33 UTC 2022-08-05 15:24:26 UTC Chemistry en Molecule 1 This dataset contains experimental data from a sample (dicopper;benzene-1,3,5-tricarboxylate, InChI=1S/2C9H6O6.2Cu/c2*10-7(11)4-1-5(8(12)13)3-6(2-4)9(14)15;;/h2*1-3H,(H,10,11)(H,12,13)(H,14,15);;/q;;2*+2/p-6).
The datasets from the following experiments are available:
X-ray diffraction (XRD)
X-ray diffraction (XRD)
single crystal X-ray diffraction (single-crystal X-ray diffraction)
https://dx.doi.org/10.14272/JMHFTDFPRQWUAN-UHFFFAOYSA-H/CHMO0000156.33 https://dx.doi.org/10.14272/JMHFTDFPRQWUAN-UHFFFAOYSA-H/CHMO0000159.16 https://dx.doi.org/10.14272/JMHFTDFPRQWUAN-UHFFFAOYSA-H/CHMO0000156.34 https://dx.doi.org/10.14272/reaction/SA-FUHFF-UHFFFADPSC-JMHFTDFPRQ-UHFFFADPSC-NUHFF-HUHFF-NUHFF-ZZZ.17

10.14272/JMHFTDFPRQWUAN-UHFFFAOYSA-H.212022-08-10T07:16:45Zpublicationpublication:samples

4.4TIB.KIT-IOC https://dx.doi.org/10.14272/JMHFTDFPRQWUAN-UHFFFAOYSA-H.21 Pilz, Lena Lena Pilz 0000-0002-5616-9003 Institute of Functional Interfaces, Karlsruhe Institute of Technology, Deutschland chemotion.net 2022 Pilz, Lena Lena Pilz 0000-0002-5616-9003 Institute of Functional Interfaces, Karlsruhe Institute of Technology, Deutschland 2022-07-28 09:29:35 UTC 2022-08-05 15:34:41 UTC Chemistry en Molecule 1 This dataset contains experimental data from a sample (dicopper;benzene-1,3,5-tricarboxylate, InChI=1S/2C9H6O6.2Cu/c2*10-7(11)4-1-5(8(12)13)3-6(2-4)9(14)15;;/h2*1-3H,(H,10,11)(H,12,13)(H,14,15);;/q;;2*+2/p-6).
The datasets from the following experiments are available:
X-ray diffraction (XRD)
X-ray diffraction (XRD)
single crystal X-ray diffraction (single-crystal X-ray diffraction)
https://dx.doi.org/10.14272/JMHFTDFPRQWUAN-UHFFFAOYSA-H/CHMO0000156.40 https://dx.doi.org/10.14272/JMHFTDFPRQWUAN-UHFFFAOYSA-H/CHMO0000156.39 https://dx.doi.org/10.14272/JMHFTDFPRQWUAN-UHFFFAOYSA-H/CHMO0000159.20 https://dx.doi.org/10.14272/reaction/SA-FUHFF-UHFFFADPSC-JMHFTDFPRQ-UHFFFADPSC-NUHFF-HUHFF-NUHFF-ZZZ.20

10.14272/JMHFTDFPRQWUAN-UHFFFAOYSA-H.202022-08-10T07:16:45Zpublicationpublication:samples

4.4TIB.KIT-IOC https://dx.doi.org/10.14272/JMHFTDFPRQWUAN-UHFFFAOYSA-H.20 Pilz, Lena Lena Pilz 0000-0002-5616-9003 Institute of Functional Interfaces, Karlsruhe Institute of Technology, Deutschland chemotion.net 2022 Pilz, Lena Lena Pilz 0000-0002-5616-9003 Institute of Functional Interfaces, Karlsruhe Institute of Technology, Deutschland 2022-07-28 09:29:17 UTC 2022-08-05 15:28:56 UTC Chemistry en Molecule 1 This dataset contains experimental data from a sample (dicopper;benzene-1,3,5-tricarboxylate, InChI=1S/2C9H6O6.2Cu/c2*10-7(11)4-1-5(8(12)13)3-6(2-4)9(14)15;;/h2*1-3H,(H,10,11)(H,12,13)(H,14,15);;/q;;2*+2/p-6).
The datasets from the following experiments are available:
X-ray diffraction (XRD)
X-ray diffraction (XRD)
single crystal X-ray diffraction (single-crystal X-ray diffraction)
https://dx.doi.org/10.14272/JMHFTDFPRQWUAN-UHFFFAOYSA-H/CHMO0000159.18 https://dx.doi.org/10.14272/JMHFTDFPRQWUAN-UHFFFAOYSA-H/CHMO0000156.37 https://dx.doi.org/10.14272/JMHFTDFPRQWUAN-UHFFFAOYSA-H/CHMO0000156.38 https://dx.doi.org/10.14272/reaction/SA-FUHFF-UHFFFADPSC-JMHFTDFPRQ-UHFFFADPSC-NUHFF-HUHFF-NUHFF-ZZZ.19 oai_datacite.f(2022-08-01T14:15:00Z).u(2022-09-01T14:20:00Z):10