Zobrazeno 1 - 10
of 204
pro vyhledávání: '"Rainer F. Winter"'
Autor:
Frank Sailer, Hipassia M. Moura, Taniya Purkait, Lars Vogelsang, Markus Sauer, Annette Foelske, Rainer F. Winter, Alexandre Ponrouch, Miriam M. Unterlass
Publikováno v:
Small Structures, Vol 5, Iss 9, Pp n/a-n/a (2024)
Hybrid materials (HMs) combine the high diversity of functionalities of organic compounds with properties typical for inorganic materials, such as high mechanical strength or high thermal stability. Herein, HMs combining organic pigment molecules and
Externí odkaz:
https://doaj.org/article/74172703fbd9427ebfc14387a6192faf
Publikováno v:
ACS Organic & Inorganic Au, Vol 4, Iss 4, Pp 395-409 (2024)
Externí odkaz:
https://doaj.org/article/c0f7810d9c66478fba3cf8880a395f48
Publikováno v:
Inorganics, Vol 11, Iss 11, p 448 (2023)
Valence tautomerism (VT) may occur if a molecule contains two chemically different redox-active units, which differ only slightly in their intrinsic redox potential. Herein, we present three new half-sandwich complexes [(η6-arene)Cr(CO)2L]+ with a t
Externí odkaz:
https://doaj.org/article/01820b4653144a8cabd4fc5d09e5bbfd
Publikováno v:
Inorganics, Vol 10, Iss 6, p 82 (2022)
We report on the tetraruthenium macrocycles Ru4-5 and -6 with a π-conjugated pyrene-appended 5,8-divinylquinoxaline ligand and either isophthalate or thiophenyl-2,5-dicarboxylate linkers and their charge-transfer salts formed by oxidation with two e
Externí odkaz:
https://doaj.org/article/92d0892789fd454f9464cdc8e6fa0dff
Publikováno v:
ACS Omega, Vol 3, Iss 8, Pp 8854-8864 (2018)
Externí odkaz:
https://doaj.org/article/4883e6d3177746a486d91cd5fc9a6956
Autor:
Nils Rotthowe, Michael Linseis, Lars Vogelsang, Nicole Orth, Ivana Ivanović-Burmazović, Rainer F. Winter
Publikováno v:
Molecules, Vol 26, Iss 17, p 5232 (2021)
Careful optimization of the reaction conditions provided access to the particularly small tetraruthenium macrocycle 2Ru2Ph-Croc, which is composed out of two redox-active divinylphenylene-bridged diruthenium entities {Ru}-1,4-CH=CH-C6H4-CH=CH-{Ru} (R
Externí odkaz:
https://doaj.org/article/960b989d84c24b50b21d4f362708b822
Publikováno v:
Inorganics, Vol 3, Iss 2, Pp 55-81 (2015)
Two pyridine-functionalized coumarins differing with respect to the site of pyridine attachment to the coumarin dye (3 in L1 or 7 in L2) and with respect to the presence (L1) or absence (L2) of a peripheral NMe2 donor were prepared and used as cyclom
Externí odkaz:
https://doaj.org/article/55db8415d89b418f932b9489372b8de8
Publikováno v:
Inorganics, Vol 6, Iss 3, p 73 (2018)
We present four new tetraruthenium macrocycles built from two 1,4-divinylphenylene diruthenium and two isophthalic acid building blocks with peripheral, potentially mono- or tridentate donor functions attached to the isophthalic linkers. These macroc
Externí odkaz:
https://doaj.org/article/70cc3948551a4a9791390a3158039ecf
Autor:
Rajorshi Das, Michael Linseis, Stefan M. Schupp, Franciska S. Gogesch, Lukas Schmidt-Mende, Rainer F. Winter
Publikováno v:
RSC Advances. 13:3652-3660
Three binary charge-transfer (CT) compounds resulting from the donor 2,2′ : 6′,2′′ : 6′′,6-trioxotriphenylamine (TOTA) and the acceptors F4TCNQ and F4BQ and of a pyrene-annulated azaacene (PAA) with the acceptor F4TCNQ are reported. The i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::64218113055a334930b993b432293b99
https://doi.org/10.1039/d2ra07322f
https://doi.org/10.1039/d2ra07322f
Autor:
Tao Jin, Lukas Kunze, Stefanie Breimaier, Michael Bolte, Hans-Wolfram Lerner, Frieder Jäkle, Rainer F. Winter, Markus Braun, Jan-Michael Mewes, Matthias Wagner
Publikováno v:
Journal of the American Chemical Society. 144:13704-13716
Polycyclic aromatic hydrocarbons (PAHs) are prominent lead structures for organic optoelectronic materials. This work describes the synthesis of three B,S-doped PAHs with heptacene-type scaffolds via nucleophilic aromatic substitution reactions betwe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a86a0b5058321d379c36a6d85be69202
https://doi.org/10.1021/jacs.2c04516
https://doi.org/10.1021/jacs.2c04516