Deuterium variable-temperature T1 measurements have been performed for a series of rhenium carbonyl clusters containing doubly and triply bridging deuterides, namely Re2(μ-D)2(CO)8 (1), Re3(μ-D)3(CO)12 (2), Re4(μ3-D)4(CO)12 (3), [NEt4][Re3(μ-D)4(CO)10] (4), [NEt4][Re3(μ-D)3(μ-Cl)(CO)10] (5), and [NEt4][Re3(μ-D)4(CO)9] (6). The deuterium quadrupolar coupling constants (DQCC) of the deuteride ligands have been evaluated for compounds 1−5, while the fluxionality of 6 hampered such a determination. The experimental DQCC of compound 3 (21.8 kHz) was, until now, the smallest found for organometallic compounds. Overall the DQCC values span a 4-fold range, and their fine-tuning depends on the bridging mode of the deuteride ligands (μ3 vs μ), the local unsaturation degree of the Re atoms bridged by the deuteride, and the presence of other bridging ligands. The experimental DQCC's of rhenium derivatives and those of bridging deuterides in Cr, W, and Os clusters linearly correlate with the respective metal−hydrogen ...