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. Author manuscript; available in PMC: 2014 Mar 4.
Published in final edited form as: Inorg Chem. 2013 Feb 22;52(5):2627–2636. doi: 10.1021/ic302543n

Table 3.

UV-Vis properties of 2•O2X, 3•O2X and 3′•O2X in CH2Cl2.

O2X λmax (nm), [ε] (M−1 cm−1)
2•O2X 3•O2X 3′•O2X
O2AsMe2 632 [2100] -- a -- b
O2PMe2 674 [1800] -- a 616 [2400]
O2PPh2 678 [2100] 621 [1800] 592 [2600]
O2P(OPh)2 680 [2800] 576 [3100] 594 [3600]
O2CCPh3 708 [2500] 630 [2200] 595 [3300]
O2CCMe3 706 [--] c 580 [3100] 577 [3800]
O2CPh 704 [--]c 588 [1500]d 592 [2300]
O2CC6H2-3,4,5-(OMe)3 707 [2600] 590 [3200] 592 [4300]
O2CC6H3-3,4-(OMe)2 704 [--]c 578 [6200] 590 [5300]
O2CC6H3-3,5-(OMe)2 706 [--]c 588 [5400] 592 [5600]
O2CC6H4-4-OMe 705 [--]c 580 [3000] 590 [4000]
a

Conversion to 3•O2X did not take place at any temperature.

b

Conversion to 3′•O2X did not take place at any temperature even with addition of 100 equivalents of OPPh3.

c

Conversion of 2•O2X to 3•O2X began before complete formation of 2•O2X, so ε was not determined.

d

Values from reference 42.