Lead—halogen bonds reactions with

In the preceding parts of Section 4.04.2.1.3 the electrophilic attack on pyrazolic nitrogen with the concomitant formation of different classes of N—R bond has been examined N—H (iv, v), N—metal (vi), N—C(sp ) (vii, viii, xi), N—C(sp ) (be, x, xi), N—SO2R (x), N—halogen (xii), N—O (xiii) and N—-N (xiv). In this last part the reaction with other Lewis acids leading to the formation of pyrazole N—metalloid bonds will be discussed, and the study of their reactivity will be dealt with in Section 4.04.2.3.lO(viii). 

Platinum removes a halogen atom from the halide, causing homolytic fission of the C-halogen bond. The resulting Pt -XR radical pair can either react to form Ptn(R)X or separate, with subsequent reaction with RX leading to either PtX2 or PtRX species or reaction with solvent molecules. 

Prior to 1958 only nitrile-adducts were reported to result from the reaction of nitriles with trihaloboranes (c.f. 36)). The first reported example of the 1,2-addition of boron-halogen bonds to a C=N group involves the reaction of tri-fluoroacetonitrile with trichloroborane or tribromoborane 4) and leads to dimeric derivatives. A 1 1 ratio of the cis-trans isomers is obtained as indicated on the basis of 19F n.m.r. studies. 

Halogen bonded to boron or carbon of the CNB grouping of the molecule seems to be of similar activity. Reactions of monomeric iminoboranes with organothiols lead to C-S substituted iminoboranes which will be discussed later (c.f. Sect. VI). 

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