Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Elias C. Rüdiger"'
Publikováno v:
Organic Materials, Vol 01, Iss 01, Pp 001-018 (2019)
Abstract Acenes have been known for a long time but their larger congeners, starphenes and phenes, have only been recently accessible as processable and characterizable derivatives. In this personalized review, we delineate the synthetic approach dev
Externí odkaz:
https://doaj.org/article/7f0f9766835a4675b3510e698325ef40
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 24(39)
Two TIPS-ethynylated dibromoacenes were used in a shotgun Yamamoto-reaction with 1,2-dibromobenzene or 4,5-dibromoveratrol. Four soluble benzononaphenes/benzoundecaphenes were isolated in satisfactory yields. Examples of tetracene- and pentacene-fuse
Autor:
Jan Freudenberg, Frank Rominger, Olena Tverskoy, Elias C. Rüdiger, Uwe H. F. Bunz, Matthias Müller, Felix Hinkel, Silke Koser
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 24(32)
The synthesis of bisalkynylated derivatives of tetrabenzo[a,c,p,r]heptacene and tetrabenzo[a,c,l,n]pentacene via two-/fourfold Stille reactions involving a 9-stannafluorene and suitable tetrabromoacenes is reported. These triphenylene-"winged" heptac
Publikováno v:
The Journal of Organic Chemistry. 81:193-196
A short synthesis of six trinaphthylenes is reported. The cyclotrinaphthylenes carry six alkoxy groups, and derivatives featuring OHex, OBu, OiPr, OPr, OEt, and OMe substituents can be obtained by an ordinary Ni(COD)2-promoted, Yamamoto-type coupling
Autor:
Uwe H. F. Bunz, Frank Rominger, Matthias Rudolph, Jürgen Schulmeister, Silke Koser, A. Stephen K. Hashmi, Thomas Wurm, Elias C. Rüdiger
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 24(11)
By employing gold catalysis, starting from dialkynylated acenes a series of novel un-symmetrical aceno-annulated dibenzopentalenes has been prepared. The achieved yields range from 62-68 %. The fused systems contain naphthalene, anthracene, tetracene
Autor:
Elias C. Rüdiger, Matthias Müller, Silke Koser, Jan Freudenberg, Frank Rominger, Uwe H. F. Bunz
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 24(5)
Triphenylene units stabilize hexacenes as dibenzo¬hex¬acenes. The hexacenes formed by a statistical Yamamoto coupling of dibromobenzene with dibromo-TIPS-pentacene or, alternatively, Stille coupling with dimethyldibenzostannole. UV-vis spectroscopy
Publikováno v:
Chemistry - A European Journal. 20:12725-12728
Two literature-known TIPS-ethynyl-dibromoacenes were prepared and employed to synthesize cyclotrimers by using Yamamoto coupling conditions. Two large, well-soluble starphenes were isolated in good yields. Crystallographic characterization verifies t
Cover Feature: Dibenzohexacene: Stabilization Through Additional Clar Sextets (Chem. Eur. J. 5/2018)
Autor:
Silke Koser, Uwe H. F. Bunz, Matthias Müller, Jan Freudenberg, Frank Rominger, Elias C. Rüdiger
Publikováno v:
Chemistry - A European Journal. 24:999-999
Autor:
Elias C. Rüdiger, Andreas Geist, Felicitas Schwörer, Udo Müllich, Petra J. Panak, Björn B. Beele
Publikováno v:
Dalton transactions (Cambridge, England : 2003). 42(34)
Two BTP-type N-donor ligands with different numbers of aromatic nitrogen atoms (2,6-bis(4-ethyl-pyridazin-1-yl)pyridine, Et-BDP and 2,6-bis(4-(n)propyl-2,3,5,6-tetrazine-1-yl)pyridine, (n)Pr-Tetrazine) have been synthesized and characterized by NMR a
Publikováno v:
Chemistry - A European Journal. 20:13036-13036