Low oxidation state s-block species Flashcards
First indications that Ae1+ compounds might be viable
From Zn chemistry
Possible to isolate formal Zn(I) compounds that contain Zn-Zn bonds using a bulky Cp* ligand
Compound can be isolated
Synthesis of Zn(I) Cp* compound
2 routes:
From Et2Zn and CpZn
OR
CpZnCl + K —> CpZn-ZnCp + KCl
First isolation of Mg(I) compound
Reduction of 2 equivalents of a beta-diketiminate Mg iodide using 2Na/K to give a Mg(I) compound with an Mg-Mg bond that can be isolated
Beta-diketiminate ligands provide kinetic stability so there is no disproportionation into Mg and M(gII)
Reactivity of soluble Mg(I) compounds
Behave as ‘bespoke’ 2-electron reducing agents
(2 electron because each Mg wants to lose one electron to form Mg2+)
Can perform organic and inorganic reductions
See flashcard
Electrides
Formed from the interaction of a crown ether/cryptand with an alkali metal at low temperature
‘Anion’ of the system is a free electron
The electron sits in voids/channels within the crystal in a ‘hydrogen-atom-like’ state i.e. the ground state of the trapped electrons is largely 1s in character
Absorption spectra of electrides
All display intense near IR absorptions that are assigned to the 1s –> 2p transition of the free electron (this is independent of the metal)
All the metals also show metal-dependent transitions that can be assigned to alkali metal anions, M-
–> = ‘alkalides’
Formation/synthesis of alkalides
Commonly formed by reduction of a less electropositive alkali metal by a more electropositive metal (i.e. a stronger reducing agent) in the presence of a crown ether or cryptand
e.g. Na + Rb + L —> [LRb]+Na-
OR
Disproportionation of the metal in the 0 oxidation state
2Na + L —> [LNa]+Na-
Uses of inorganic electrides
The ‘disproportionation chemistry’ of Na doesn’t just happen in liquid NH3 - can also happen in zeolites/silica gel when impregnated with Na metal
Can be used as heterogenised sources of electrode materials for carrying out reduction reactions