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Type |
Poster Presentation |
Area |
Inorganic Chemistry |
Room No. |
Event Hall |
Time |
4월 19일 (목요일) 11:00~12:30 |
Code |
INOR.P-67 |
Subject |
Synthesis and Photoreaction of adsorbed diiodomethane of Neutral Pd(II) Complexes |
Authors |
Dongwon Kim, Seo Young Hwang1, Ok-Sang Jung1,* Department of chemistry, Pusan National University, Korea 1Department of Chemistry, Pusan National University, Korea |
Abstract |
A series of Pd6L4-type neutral coordination cages, [Pd6X12L4] (X- = Cl- and Br-), are constructed via self-assembly of (COD)PdCl2 and K2PdBr4 with C3-symmetric N,N′,N′′-tris(2-pyridinylmethyl)-1,3,5-benzenetricarboxamide (L), respectively. The iodide analogue [Pd6I12L4] is smoothly synthesized from [Pd6Br12L4] in the presence of CH2I2 under mild conditions. The replacement of bromide to iodide in the nanocage system represents a landmark achievement in synthetic-methodology development. The CH2I2 molecules are adsorbed in the order [Pd6I12L4] > [Pd6Br12L4] > [Pd6Cl12L4] and in the “like-attracts-like” pattern, presumably owing to the van der Waals force. Irradiation of [Pd6I12L4]·3.5CH2I2 with 1-methylcyclohexene in chloroform at 350 nm preferentially affords the cyclopropanation product.
Reference
[1] Noh, T. H.; Lee, H.; Kim, D.; Moon, D.; Lee, Y.-A.; Jung, O.-S. Dalton Transactions. , 2016, 45, 9574-9581.
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E-mail |
zxcv764@naver.com |
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