“…Yield: 0.015 g (72%). 1 H NMR (400 MHz, DMSO) d 13.12 (s, 1H N-H ) 9.54 (dd, 3 J HH = 4.2, 1.1 Hz, 1H pyz ), 9.27 (d, 3 J HH = 1.0 Hz, 1H pyz ), 9.12 (d, 3 J HH = 3.0 Hz, 1H bz ), 7.75 (dd, 3 J HH = 3.2 Hz, 2H bz ), 7.45 (dd, 3 J HH = 3.0, 2.7 Hz, 2H bz ), 6.20 (d, 3 J HH = 6.0 Hz, 1H, cymene CH), 6.09 (d, 3 J HH = 6.0 Hz, 1H, cymene CH), 6.04 (d, 3 J HH = 6.0 Hz, 1H, cymene CH), 5.95 (d, J HH = 6.0 Hz, 1H, cymene CH 2 ), 2.63 (sept, 3 J HH = 7.2 Hz, 1H, CHMe 2 ), 2.24 (s, 3H, Me), 1.11 (d, 3H, CHMe 2 ), 1.01 (d, 3H, CHMe 2 ), 13 -(benzo[d]thiazol-2-yl)pyrazine-2carboxamide)Cl] (Ru2). Complex Ru2 was prepared following the procedure described for Ru1 using N-(benzo[d]thiazol-2-yl) pyrazine-2-carboxamide (L2 (0.01 g, 0.04 mmol) and dichloro(p-cymene)ruthenium(II) dimer (0.05 g, 0.08 mmol).…”