Despite the large body of work on {Ru(bpy)} sensitizer fragments, the same attention has not been devoted to their {Ru(py)} analogues. In this context, we explored the donor-acceptor trans-[Ru(L){(μ-NC)Cr(CN)}], where L = pyridine, 4-methoxypyridine, 4-dimethylaminopyridine. We report on the synthesis and the crystal structure as well as the electrochemical, spectroscopical, and photophysical properties of these trimetallic complexes, including transient absorption measurements. We observed emission from chromium-centered d-d states upon illuminating into either MLCT or MM'CT absorptions of {Ru(L)} or {Ru-Cr}, respectively. The underlying energy transfer is as fast as 600 fs with quantum efficiencies ranging from 10% to 100%. These results document that {Ru(py)} sensitizer fragments are as efficient as {Ru(bpy)} in short-range energy transfer scenarios.