254101-30-9Relevant academic research and scientific papers
Cross-conjugated bis(porphryin)s: Synthesis, electrochemical behavior, mixed valency, and biradical dication formation
Shultz, David A.,Lee, Hyoyoung,Kumar, R. Krishna,Gwaltney, Kevin P.
, p. 9124 - 9136 (1999)
The synthesis and characterization of seven (Zn(II))2bis(porphyrin) molecules are described. The molecular structures of two bis(porphyrin)s'(6 and 7) were determined by X-ray diffraction methods. Four of the compounds have their porphyrin moie
Lithium halide ion-pair recognition with halogen bonding and chalcogen bonding heteroditopic macrocycles
Tse, Yuen Cheong,Docker, Andrew,Zhang, Zongyao,Beer, Paul D.
, p. 4950 - 4953 (2021)
A series of halogen bonding and chalcogen bonding phenanthroline containing heteroditopic macrocyclic receptors exhibit cooperative recognition of lithium halide (LiX) ion-pairs. Quantitative 1H NMR ion-pair titration experiments in CDCl3?:?CD3CN (1?:?1,
A Halogen-Bond-Induced Triple Helicate Encapsulates Iodide
Massena, Casey J.,Wageling, Nicholas B.,Decato, Daniel A.,Martin Rodriguez, Enrique,Rose, Ariana M.,Berryman, Orion B.
, p. 12398 - 12402 (2016/10/13)
The self-assembly of higher-order anion helicates in solution remains an elusive goal. Herein, we present the first triple helicate to encapsulate iodide in organic and aqueous media as well as the solid state. The triple helicate self-assembles from thre
Aromatic and aliphatic CH hydrogen bonds fight for chloride while competing alongside ion pairing within triazolophanes
Hua, Yuran,Ramabhadran, Raghunath O.,Uduehi, Esther O.,Karty, Jonathan A.,Raghavachari, Krishnan,Flood, Amar H.
supporting information; experimental part, p. 312 - 321 (2011/03/21)
Triazolophanes are used as the venue to compete an aliphatic propylene CH hydrogen-bond donor against an aromatic phenylene one. Longer aliphatic C-H...Cl- hydrogen bonds were calculated from the location of the chloride within the propylene-ba
