216683-34-0Relevant academic research and scientific papers
Selective anion binding and solid-state host-guest chemistry of an extended cavity calix[6]pyrrole
Turner,Shterenberg,Kapon,Suwinska,Eichen
, p. 13 - 14 (2001)
Easily prepared, cone-like, extended cavity calix[6]pyrrole is shown to form strong complexes with iodine and other halide ions as well as with trihaloalkanes and electron deficient aromatic systems.
Biladiene type rare earth complex as well as preparation method and application thereof
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Paragraph 0053-0056, (2021/05/19)
The invention discloses a biladiene type rare earth complex and a preparation method and application thereof. The structural formula of the biladiene type rare earth complex is shown in the specification, R is an electron withdrawing group, and Ln is a la
Selective ethylene tri-/tetramerization by in situ-formed chromium catalysts stabilized by N,P-based ancillary ligand systems
Yang, Yun,Liu, Zhen,Liu, Boping,Duchateau, Robbert
, p. 2353 - 2361 (2013/10/22)
A series of N,P-based ancillary ligands have been synthesized, and the corresponding catalysts, formed in situ by mixing one of the N,P-ligands, Cr(acac)3 and MAO, have been tested for ethylene oligomerization. Under standard ethylene oligomeri
5,5-Diaryldipyrromethanes: Syntheses and anion binding properties
Gowri Sreedevi,Thomas, Ajesh P.,Salini,Ramakrishnan,Anju,Derry Holaday,Reddy,Suresh,Srinivasan
supporting information; experimental part, p. 5995 - 5999 (2011/11/28)
A two-step synthesis of 5,5-diaryldipyrromethanes in good yields is described. The adopted synthetic strategy can be used to tune the substituent at the meso-carbon very easily by choosing the Grignard reagent of interest. Further, the influence of the in
Extended calixpyrroles: Meso-substituted calix[6]pyrroles
Turner, Boaz,Botoshansky, Mark,Eichen, Yoav
, p. 2475 - 2428 (2007/10/03)
A 1,3,5-alternate conformation of the pyrrole rings is adopted by the calix[6]pyrrole 1 in the crystal (see picture). Compound 1 was synthesized in a two-step process and although it crystallizes in the form of the adduct 1.3CH3COCH3
