Abstract
A tetrameric metallocycle [Pd(dppp)(DPNDI)]4·8TfO consisting of four dppp-capped Pd(II) corners (dppp = 1,3-bis(diphenylphosphonium)propane) and four linear π-acidic N,N′-di(4-pyridyl)-1,4,5,8-naphthalene diimine (DPNDI) ligands has been synthesized, and its single-crystal structure has been elucidated for the first time. The crystal structure of the metallocycle revealed anion-π, lone-pair-π, and CH···anion interactions between electron-deficient DPNDI ligands and TfO- counterions and provided valuable insights into its anion recognition and metathesis capabilities. The 1H, 19F, and 31P NMR studies demonstrated that in noncoordinating solvents, such as nitromethane and dichloromethane, the [Pd(dppp)(DPNDI)]4 8+ metallocycle underwent anion exchange in a single-crystal to single-crystal fashion without any structural changes. However, the metallocycle experienced slow dissociation in a polar solvent DMSO, which could be reversed easily by thermal treatment.
| Original language | English |
|---|---|
| Pages (from-to) | 6017-6022 |
| Number of pages | 6 |
| Journal | Crystal Growth and Design |
| Volume | 19 |
| Issue number | 11 |
| DOIs | |
| State | Published - 6 Nov 2019 |
| Externally published | Yes |
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