37067-12-2Relevant academic research and scientific papers
Substituted phenanthrolines as antennae in luminescent EuIII complexes
Akerboom, Sebastiaan,Van Den Elshout, Jos J. M. H.,Mutikainen, Ilpo,Siegler, Maxime A.,Fu, Wen Tian,Bouwman, Elisabeth
, p. 6137 - 6146 (2014/01/06)
Eight novel europium(III)-based coordination compounds with 1,10-phenanthroline (phen) ligands with a chloro, methoxy, ethoxy, cyano, carboxylic acid, methyl carboxylate, ethyl carboxylate, and amino substituent on the 2-position have been prepared in yields ranging from 43 to 89 %. Additionally, one lanthanum(III) coordination compound of 2-amino-1,10- phenanthroline has been isolated. All compounds have the general formula [Ln(L)2(NO3)3], except for the compound with the carboxylate ligand, which has the formula [Eu(O2Cphen) 3]. Three of the EuIII complexes as well as the La III compound crystal structures have been determined, all of which show similar N4O6 coordination spheres for the Ln III ion. Seven compounds exhibit bright luminescence that is characteristic of EuIII upon irradiation with near-UV radiation, thus indicating efficient ligand-to-metal energy transfer. The complex with 2-amino-1,10-phenanthroline is nonluminescent. The solid-state photoluminescent quantum yields range from 10 to 79 %, and the luminescence lifetimes vary from 0.43 to 1.57 ms. Analysis of the spectral intensities with the Judd-Ofelt theory shows a significant contribution of nonradiative processes that quench the luminescence of the 5D0 level on EuIII. Eight new EuIII complexes with 1,10-phenanthroline ligands substituted on the 2-position have been prepared, analyzed, and the photoluminescence properties studied. The complex with the 2-chloro substituent exhibits bright photoluminescence with a high quantum yield of 78 %. The complex with the 2-amino substituent is nonluminescent. Copyright
Electronically variable imino-phenanthrolinyl-cobalt complexes; synthesis, structures and ethylene oligomerisation studies
Pelletier, Jérémie D.A.,Champouret, Yohan D.M.,Cadarso, Jesus,Clowes, Lucy,Ga?ete, Marcos,Singh, Kuldip,Thanarajasingham, Vakesan,Solan, Gregory A.
, p. 4114 - 4123 (2007/10/03)
The 2-imino-1,10-phenanthroline ligands, 1,10-C12H7N2-2-CR{double bond, long}N(2,6-i-Pr2-4-R1-C6H2) [R = R1 = H (L1); R = H, R1 = Br (L2); R = H, R1 = CN (L3); R = H, R1 = i-Pr (L4); R = Me, R1 = H (L5); R = Me, R1 = i-Pr (L6)], have been prepared in high yield from the condensation reaction of 1,10-C12H7N2-2-CR{double bond, long}O (R = H, Me) with one equivalent of the corresponding 4-substituted 2,6-diisopropylaniline. The molecular structures of L2, L5 and L6 reveal the imino nitrogen atoms to adopt a transoid configuration with respect to the phenanthrolinyl nitrogen atoms. Treatment of Lx with one equivalent of CoCl2 in n-BuOH at 90 °C gives the high spin complexes, (Lx)CoCl2 [Lx = L1 (1a), L2 (1b), L3 (1c), L4 (1d), L5 (1e), L6 (1f)], in which the metal centres exhibit distorted square pyramidal geometries. Activation of 1a-1f with excess methylaluminoxane (MAO) gives catalysts that are modestly active for the oligomerisation of ethylene affording mainly linear α-olefins along with some degree of internal olefins. While the donor capability of the 4-position of the N-aryl group does not appear to affect the activity of the catalyst, it does have an influence on the ratio of α-olefins to internal olefins. Single crystal X-ray diffraction studies have been performed on L2, L5, L6, 1a, 1c and 1f.
Carboxylic and Phosphate Ester Hydrolysis Catalysed by Bivalent Zinc and Coper Metallosurfactants
Weijnen, John G. F.,Koudijs, Arie,Engbersen, Johan F. J.
, p. 1121 - 1126 (2007/10/02)
The synthesis of three new lipophilic ligands are reported: Nα-(1,10-phenanthrolin-2-ylmethyl)-N-τ-dodecylhistamine (1), N-dodecyl-2-aminomethyl-1,10-phenanthroline (2), and Nα-(2-pyridylmethyl)-Nτ-dodecylhistam
