New Di- and Triorganotin(IV) Tyrosylalaninates as Models for
Metal—Protein Interactions: Synthesis, Structural Characterization, and Potentiometric Studies of Tyrosylalanine, Glycyltyrosine, and Glycylisoleucine with Di- and Trimethyltin(IV) Moieties in Aqueous Medium
Table 2
IR frequenciesa (in cm−1) of di- and triorganotin(IV) tyrosylalaninates.
Compound
ν(O–H)
ν(N–H)/ν(C–H)
(COO)/(COO)
Δν
(Sn–C)/(Sn–C)
ν(Sn–O)/ν(Sn←N)
H2Tyr-Ala
3440 m 3180 br
1670
1560 m 1390 m
170
—
—
Me2Sn(Tyr-Ala)
3516 m
3380 m 3286 m 3230 w 3177 m 2924 w
1594 vs
1514 m/1340 w 1291 w
174
592 m/523 m
551 m/489 w
n-Bu2Sn(Tyr-Ala)
3566 m
3427 s 3343 s 3239 w 3187 s
1655 s
1622 vs/1369 w
253
671 m/587 m
557 m/451 m
n-Oct2Sn(Tyr-Ala)
3586 m
3412 m 3270 m 3227 m 3014 w
1640 brsh
1610 vs/1379 m
231
677 m/555 s
570 w/452 vw
Ph2Sn(Tyr-Ala)
3571 s
3424 s 3333 s 3231 w 3194 s
1633 vs
1615 s/1397 m
218
247 m/226 m
533 m/457 m
Me3Sn(HTyr-Ala)
3439 br
3332 s 3265 s 3101 s
1659 m
1602 vs/1394 m
208
607 w/591 w
545 m/424 m
Ph3Sn(HTyr-Ala)
3457 s
3344 s 3171 s 3055 s
1660 vs
1526 s/1250 s
276
280 m/228 w
503 m/449 m
avs, very strong; s, strong; m, medium; w, weak; br, broad.