Informationen zur Darstellung dieser Seite in älteren Browsern
Index Name
Marder, Todd B.
Alternative Writings
Marder, T.B.
Co-authors
Albesa-Jove, David;
Albesa-Jové, David;
Batsanov, Andrei S.;
Beeby, Andrew;
Borwick, Simon;
Bruce, Duncan W.;
Burke, Jacqueline M.;
Burke, Jacquelyn M.;
Chu, Vano;
Clark, Stewart J.;
Clegg, William;
Collings, Jonathan C.;
Dai, Chaoyang;
Fasina, Tolulope M.;
Howard, Judith A.K.;
Ledoux, Isabelle;
Lesley, Gerry;
Low, Paul J.;
Lydon, Donocadh P.;
Nguyen, Paul;
Porres, Laurent;
Robins, Edward G.;
Rourke, Jonathan P.;
Scott, Andrew J.;
Seddon, John M.;
Shearman, Gemma C.;
Smith, Caroline E.;
Smith, Philip S.;
Taylor, Nicholas J.;
Thomas, Rhodri Ll.;
Viney, Christopher;
Ward, Richard M.;
Watt, Stephen W.;
Zyss, Joseph
Publication Titles
1994: Organometallic liquid crystals based on octahedral rhodium(III)
1995: Well-defined conjugated rigid-rods as multifunctional materials: Linear and nonlinear optical properties and liquid crystalline behavior
1997: Second-Order Nonlinear Optical Properties of Push-Pull Bis(phenylethynyl)benzenes and Unsymmetric Platinum Bis(phenylacetylide) Complexes
1999: Control of single crystal structure and liquid crystal phase behaviour via arene-perfluoroarene interactions
2004: Arene-perfluoroarene interactions in crystal engineering: structural preferences in polyfluorinated tolans
2004: Structure and phase behavior of a 2:1 complex between arene- and fluoroarene-based conjugated rigid rods
2005: A simple "palladium-free" synthesis of phenyleneethynylene-based molecular materials revisited
2005: Synthesis, optical properties, crystal structures and phase behaviour of symmetric, conjugated ethynylarene-based rigid rods with terminal carboxylate groups
2008: The synthesis and liquid crystalline behaviour of alkoxy-substituted derivatives of 1,4-bis(phenylethynyl)benzene
Sources
Angew. Chem., Int. Ed., 43, 3061
Chem. Commun., 1999, 2493
Chem. Mater., 9, 406
J. Chem. Soc., Dalton Trans., 1994, 317
J. Mater. Chem., 14, 413
J. Mater. Chem., 15, 690
Liq. Cryst., 35, 119
NATO ASI Ser. E, 297, 333
New J. Chem., 29, 972