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. Author manuscript; available in PMC: 2010 Sep 6.
Published in final edited form as: Chem Res Toxicol. 2010 Feb 15;23(2):413–421. doi: 10.1021/tx900372p

Table 1. Structures of complexes discussed in this work.

Complex
Ligand TRANS CIS
‘X’ graphic file with name ukmss-31748-t0012.jpg graphic file with name ukmss-31748-t0013.jpg
NH3 1t [a] 1c
MeNH2 2t [b] N/A
EtNH2 3t [b] N/A
PrNH2 N/A 4c
BuNH2 N/A 5c
PentNH2 N/A 6c
Py
graphic file with name ukmss-31748-t0014.jpg
7t [a] 7c
2-methylpyridine
graphic file with name ukmss-31748-t0015.jpg
8t [b] 8c
3-methylpyridine
graphic file with name ukmss-31748-t0016.jpg
9t [b] 9c
4-methylpyridine
graphic file with name ukmss-31748-t0017.jpg
10t N/A
2-bromo,3-
methylpyridine
graphic file with name ukmss-31748-t0018.jpg
11t N/A
[a]

Synthesis and cytotoxicity data previously reported: 1t (19), 7t (11).

[b]

Synthesis previously reported (21).