نتایج جستجو برای: bulky ω aryloxyalkyl substituted indenyl ligands

تعداد نتایج: 174990  

Journal: :Advanced Energy Materials 2022

Quasi-2D hybrid halide perovskites have drawn considerable attention due to their improved stability and facile tunability compared 3D perovskites. The expansiveness of possibilities has thus far been limited by the difficulty in incorporating large ligands into thin-film devices. Here, a bulky bi-thiophene 2T ligand is focused on develop solvent system around creating strongly vertically-align...

Journal: :Journal of materials chemistry. A, Materials for energy and sustainability 2021

The utilization of alkylamino-substituted terephthalic ligands is demonstrated as an efficient synthetic strategy towards microporous 8-connected Zr4+ MOFs, which were proved to be the most sorbents for Se toxic anions ever reported.

2000
Balázs Dóra Kazumi Maki Attila Virosztek

– We study theoretically the optical conductivity of d-wave superconductors like in high temperature cuprates in the presence of impurities. We limit ourselves at T = 0K and focus on the frequency dependence of both σ1(ω) and ωσ2(ω) for ω . 2∆. When the impurity scattering is in the unitary limit, we find a peak in σ1(ω) with ω/∆ ≃ 0.1 ∼ 0.5, which may account for the peak seen by Basov et al. ...

Journal: :Dalton transactions 2004
Francesca M Kerton Adrian C Whitwood Charlotte E Willans

Libraries of lanthanide complexes supported by nitrogen and oxygen containing ligands have been synthesised using a high-throughput approach. The complexes were employed in the ring-opening polymerisation of epsilon-caprolactone, in some cases giving polycaprolactone of controlled molecular weight and narrow polydispersity. The libraries, based on twenty-one ligands and eight lanthanide reagent...

Journal: :Chemical communications 2002
Yong-Gui Zhou Xumu Zhang

Some novel ortho-substituted BINOL-derived bisphosphorous ligands (o-BINAPO and o-NAPHOS) were synthesis from readily available (S)-BINOL; these ligands showed excellent enantioselectivities (up to 99% ee) in Rh(I)-catalyzed asymmetric hydrogenation of functionalized olefins.

Journal: :Dalton transactions 2013
Daniele Anselmo Rafael Gramage-Doria Tatiana Besset Martha V Escárcega-Bobadilla Giovanni Salassa Eduardo C Escudero-Adán Marta Martínez Belmonte Eddy Martin Joost N H Reek Arjan W Kleij

The use of the commercially available, bifunctional phosphine 1,3,5-triaza-7-phosphaadamantane (abbreviated as PN3) in conjunction with a series of Zn(salphen) complexes leads to sterically encumbered phosphine ligands as a result of (reversible) coordinative Zn-N interactions. The solid state and solution phase behaviour of these supramolecular ligand systems have been investigated in detail a...

A series of 8 new complexes of titanium and zirconium with diamido ligands bearing an ethylene and propylene bridge between the two amido groups were synthesized and tested for ethylene polymerization. Titanium complexes bearing an ethylene bridge between the two amido groups showed higher activities than the derivatives with a propylene bridge. In the case of the zirconium complexes, the p...

2015
Jeffrey D. Klenc JEFFREY D. KLENC Lucjan Strekowski Alfons Baumstark Markus Germann

Novel and potent ligands to the serotonin7 (5-HT7) receptor have been synthesized. The synthesized compounds include a set of substituted pyrimidines which show high affinity to the 5-HT7 receptor, synthesized by previously described methods [1,2] in high yield. Comparing the affinities of substituted pyrimidines to previously calculated models [3,4] yielded new hypotheses about the nature of i...

Journal: :Molecules 2013
Andrijana Meščić Svjetlana Krištafor Ivana Novaković Amar Osmanović Ursina Müller Davorka Završnik Simon M Ametamey Leonardo Scapozza Silvana Raić-Malić

The efficient syntheses of 5-(2-hydroxyethyl)- and 5-(3-hydroxypropyl)-substituted pyrimidine derivatives bearing 2,3-dihydroxypropyl, acyclovir-, ganciclovir- and penciclovir-like side chains are reported. A synthetic approach that included the alkylation of an N-anionic-5-substituted pyrimidine intermediate (method A) provided the target acyclonucleosides in significantly higher overall yield...

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