There is considerable evidence that SN1 mechanism is followed in diazo aromatic compounds' nucleophilic substitution. I would like to know the reason for this and why is it preferred to SNAr mechanism even when the $\ce{N2+}$ could stabilize the carbanion-type intermediate through -I effect.
Does it have to do with the excellent leaving tendency of $\ce{N2+}$ but at the cost of formation of unstable phenyl cation?