Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Morten K Peters"'
Publikováno v:
Acta Crystallographica Section E: Crystallographic Communications, Vol 75, Iss 6, Pp 925-929 (2019)
The asymmetric unit of the title compound, [Ni(C52H34Cl4N4O4)]·CH2Cl2, consists of two discrete complexes, which show significant differences in the conformation of the side chain. Each NiII cation is coordinated by four nitrogen atoms of a porphyri
Externí odkaz:
https://doaj.org/article/57eefa2eec0145af83284c7a9c563be7
Publikováno v:
Acta Crystallographica Section E: Crystallographic Communications, Vol 75, Iss 6, Pp 930-933 (2019)
The title compound, [Fe2(C44H28N4O)2O], was obtained as a by-product during the synthesis of FeIII tetraphenylporphyrin perchlorate. It crystallizes as a new polymorphic modification in addition to the orthorhombic form previously reported [Hoffman e
Externí odkaz:
https://doaj.org/article/7b65cde93729468ab1adf796a451f73e
Publikováno v:
Acta Crystallographica Section E: Crystallographic Communications, Vol 75, Iss 6, Pp 762-765 (2019)
In the crystal structure of the title compound, [Fe(C44H28N4)(C6H7NO)2]ClO4, the FeIII ions are coordinated in an octahedral fashion by four N atoms of the porphyrin moiety and two N atoms of two 4-methoxypyridine ligands into discrete complexes that
Externí odkaz:
https://doaj.org/article/4fc3a8a46665450bb119cd37b93f3021
Publikováno v:
Acta Crystallographica Section E: Crystallographic Communications, Vol 74, Iss 7, Pp 1013-1016 (2018)
The crystal structure of the title compound, C11H10N4, comprises molecules in a trans conformation for which all the atoms are located in general positions. The six-membered rings are coplanar and this arrangement might be stabilized by intramolecula
Externí odkaz:
https://doaj.org/article/889998ae62bd4d60a0f0e560cdecf207
Autor:
Morten K. Peters, Rainer Herges
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 13, Iss 1, Pp 2659-2662 (2017)
The synthesis, isolation and characterization of isobenzofuran are described in this publication. Isobenzofuran is of general interest in synthetic and physical organic chemistry because it is one of the most reactive dienes known. A number of synthe
Externí odkaz:
https://doaj.org/article/7e203682eded44d690b1d8d8d185330f
Autor:
Jens Gröbner, Jannis Ludwig, Lukas Huber, Morten K Peters, Rainer Herges, Marcel Dommaschk, Jan-Bernd Hövener
Publikováno v:
Journal of Porphyrins and Phthalocyanines. 24:480-488
A water-soluble Ni(II)-porphyrin substituted with a covalently attached azopyridine ligand was synthesized. Upon irradiation with violet and green light, the azo unit performs a reversible cis–trans isomerization. This geometry change triggers a co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::208ed8e8e017e3722aa7f260dd6d9e0b
https://doi.org/10.1142/s1088424619501803
https://doi.org/10.1142/s1088424619501803
Publikováno v:
Acta Crystallographica Section E: Crystallographic Communications, Vol 75, Iss 6, Pp 930-933 (2019)
The title compound, [Fe2(C44H28N4O)2O], was obtained as a by-product during the synthesis of FeIII tetraphenylporphyrin perchlorate. It crystallizes as a new polymorphic modification in addition to the orthorhombic form previously reported [Hoffman e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cd0e51b20143f3390c85bf3a4b2934f3
https://doi.org/10.1107/s2056989019007576
https://doi.org/10.1107/s2056989019007576
Publikováno v:
Acta Crystallographica Section E: Crystallographic Communications
Acta Crystallographica Section E: Crystallographic Communications, Vol 75, Iss 6, Pp 762-765 (2019)
Acta Crystallographica Section E: Crystallographic Communications, Vol 75, Iss 6, Pp 762-765 (2019)
In the crystal structure of the title compound, the FeIII ions are octahedrally coordinated by four N atoms of a porphyrin moiety as well as two 4-methoxypyridine ligands into discrete complexes that are charge-balanced by perchlorate anions.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d34810f735936300701297e82b87fdfe
http://europepmc.org/articles/PMC6658977
http://europepmc.org/articles/PMC6658977
Autor:
Christian Naether, Morten K Peters, Fynn Röhricht, Frank D. Sönnichsen, Rainer Herges, Kari Rissanen, Manu Lahtinen, Sebastian Hamer, Carolina von Essen, Torben Jäkel
Publikováno v:
Inorganic Chemistry. 58(8):5265-5272
Fe(III) porphyrins bridged with 1,2,3-triazole ligands were synthesized. Upon deprotonation, the triazolate ion coordinates to the Fe(III) ion, forming an overall neutral high-spin Fe(III) porphyrin in which the triazolate serves both as an axial lig
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::38557167519141c49bcced0075d47a84
https://doi.org/10.1021/acs.inorgchem.9b00349
https://doi.org/10.1021/acs.inorgchem.9b00349
Publikováno v:
Acta Crystallographica Section E: Crystallographic Communications, Vol 74, Iss 7, Pp 1013-1016 (2018)
Acta Crystallographica Section E: Crystallographic Communications
Acta Crystallographica Section E: Crystallographic Communications
In the crystal structure of the title compound the molecules are coplanar and are linked into helical chains via N—H⋯N hydrogen bonding between one of the amino H atoms and the pyridine N atoms.
The crystal structure of the title compound,
The crystal structure of the title compound,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3972c49eda86aa0d637bd6e1c849fa84
https://doi.org/10.1107/s2056989018008605
https://doi.org/10.1107/s2056989018008605