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Literature DB >> 19016279

Reversible "chiral memory" in ruthenium tris(phenanthroline)-anionic porphyrin complexes.

Rosalba Randazzo¹, Angela Mammana, Alessandro D'Urso, Rosaria Lauceri, Roberto Purrello.

Abstract

Entities: Chemical

Mesh：

Substances：

Year: 2008 PMID： 19016279 DOI： 10.1002/anie.200803619

Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN： 1433-7851 Impact factor: 15.336

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7 in total

1. Selection of supramolecular chirality by application of rotational and magnetic forces.

Authors: N Micali; H Engelkamp; P G van Rhee; P C M Christianen; L Monsù Scolaro; J C Maan
Journal: Nat Chem Date: 2012-02-12 Impact factor: 24.427

2. Switchable enantioseparation based on macromolecular memory of a helical polyacetylene in the solid state.

Authors: Kouhei Shimomura; Tomoyuki Ikai; Shigeyoshi Kanoh; Eiji Yashima; Katsuhiro Maeda
Journal: Nat Chem Date: 2014-04-13 Impact factor: 24.427

3. trans-{1,8-Bis[(S)-1-phenyl-eth-yl]-1,3,6,8,10,13-hexa-aza-cyclo-tetra-deca-ne}bis(thio-cyanato--κN)copper(II).

Authors: Jong Won Shin; Sankara Rao Rowthu; Jae Jeong Ryoo; Kil Sik Min
Journal: Acta Crystallogr Sect E Struct Rep Online Date: 2010-07-10

4. Controlling J-Aggregates Formation and Chirality Induction through Demetallation of a Zinc(II) Water Soluble Porphyrin.

Authors: Ilaria Giuseppina Occhiuto; Maria Angela Castriciano; Mariachiara Trapani; Roberto Zagami; Andrea Romeo; Robert F Pasternack; Luigi Monsù Scolaro
Journal: Int J Mol Sci Date: 2020-06-03 Impact factor: 5.923

Reversible "chiral memory" in ruthenium tris(phenanthroline)-anionic porphyrin complexes.

1. Selection of supramolecular chirality by application of rotational and magnetic forces.

2. Switchable enantioseparation based on macromolecular memory of a helical polyacetylene in the solid state.

3. trans-{1,8-Bis[(S)-1-phenyl-eth-yl]-1,3,6,8,10,13-hexa-aza-cyclo-tetra-deca-ne}bis(thio-cyanato--κN)copper(II).

4. Controlling J-Aggregates Formation and Chirality Induction through Demetallation of a Zinc(II) Water Soluble Porphyrin.

5. Homochiral self-assembly of biocoordination polymers: anion-triggered helicity and absolute configuration inversion.

6. Design principles of chiral carbon nanodots help convey chirality from molecular to nanoscale level.

7. Chaperone-like chiral cages for catalyzing enantio-selective supramolecular polymerization.