Divergent reactivity of 2-vinylpyridine and 1-vinylpyrazole in rhodium-phosphine systems: C-H activation and dinuclear chemistry

The Rh-I-Rh-III mixed valence dinuclear complex Rh-2-Cl-2(mu-H)(mu-eta(2),kappa(2)-C, N-NC5H4-2-(Z)CH=CH)( PPhMe2)(3) has been prepared by reaction of [Rh(mu-Cl)(eta(2)-coe)(2)](2) with 2-vinylpyridine in the presence of dimethylphenylphosphine as a result of C-H activation of the terminal olefinic proton. The X- ray structure presents anagostic Rh center dot center dot center dot HC and pi-pi interactions between aromatic rings. In contrast, 1-vinylpyrazole does not undergo a C-H activation process, resulting in the formation of dinuclear species supported by 1 vinylpyrazole bridges. Anagostic Rh center dot center dot center dot HC interactions and CH center dot center dot center dot Cl hydrogen bonds are responsible for the 3D packing of the complex. El complejo dinuclear de valencia mixta RhI-RhIII Rh2-Cl2(µ-H)(µ-¿2,¿2-C,N-NC5H4-2-(Z)CH=CH)(PPhMe2)3 ha sido preparado por reacción de [Rh(µ-Cl)(¿2-coe)2]2 con 2-vinilpiridina en presencia de dimetilfenilfosfina, como resultado de la activación C-H del protón terminal de la olefina. La estructura de rayos-X presenta enlaces anagósticos Rh···HC, así como interacciones p-p entre anillos aromáticos. Por otro lado, la reacción con 1-vinilpirazol no da lugar a una activación C-H sino que se observa la formación de una especie dinuclear soportada por ligandos 1-vinilpirazol puente. Diferentes interacciones anagósticas Rh···HC y de enlace de hidrógeno CH···Cl son responsables del empaquetamiento tridimensional del complejo

Preparation of Butadienylpyridines by Iridium-NHC-Catalyzed Alkyne Hydroalkenylation and Quinolizine Rearrangement

Iridium(I) N-heterocyclic carbene complexes of formula Ir(¿2O, O’-BHetA)(IPr)(¿2-coe) [BHetA=bis-heteroatomic acidato, acetylacetonate or acetate; IPr=1, 3-bis(2, 6-diisopropylphenyl)imidazolin-2-carbene; coe=cyclooctene] have been prepared by treating Ir(¿2O, O’-BHetA)(¿2-coe)2 complexes with IPr. These complexes react with 2-vinylpyridine to afford the hydrido-iridium(III)-alkenyl cyclometalated derivatives IrH(¿2O, O’-BHetA)(¿2N, C-C7H6N)(IPr) through the iridium(I) intermediate Ir(¿2O, O’-BHetA)(IPr)(¿2-C7H7N). The cyclometalated IrH(¿2O, O’-acac)(¿2N, C–C7H6N)(IPr) complex efficiently catalyzes the hydroalkenylation of aromatic and aliphatic terminal alkynes and enynes with 2-vinylpyridine to afford 2-(4R-butadienyl)pyridines with Z, E configuration as the major reaction products (yield up to 89 %). In addition, unprecedented (Z)-2-butadienyl-5R-pyridine derivatives have been obtained as minor reaction products (yield up to 21 %) from the elusive 1Z, 3gem-butadienyl hydroalkenylation products. These compounds undergo a thermal 6p-electrocyclization to afford bicyclic 4H-quinolizine derivatives that, under catalytic reaction conditions, tautomerize to 6H-quinolizine to afford the (Z)-2-(butadienyl)-5R-pyridine by a retro-electrocyclization reaction. © 2021 The Authors. Chemistry - A European Journal published by Wiley-VCH Gmb

Preparation of Butadienylpyridines by Iridium‐NHC‐Catalyzed Alkyne Hydroalkenylation and Quinolizine Rearrangement

Iridium(I) N‐heterocyclic carbene complexes of formula Ir(κ(2) O,O’‐BHetA)(IPr)(η (2)‐coe) [BHetA=bis‐heteroatomic acidato, acetylacetonate or acetate; IPr=1,3‐bis(2,6‐diisopropylphenyl)imidazolin‐2‐carbene; coe=cyclooctene] have been prepared by treating Ir(κ(2) O,O’‐BHetA)(η (2)‐coe)(2) complexes with IPr. These complexes react with 2‐vinylpyridine to afford the hydrido‐iridium(III)‐alkenyl cyclometalated derivatives IrH(κ(2) O,O’‐BHetA)(κ(2) N,C‐C(7)H(6)N)(IPr) through the iridium(I) intermediate Ir(κ(2) O,O’‐BHetA)(IPr)(η (2)‐C(7)H(7)N). The cyclometalated IrH(κ(2) O,O’‐acac)(κ(2) N,C–C(7)H(6)N)(IPr) complex efficiently catalyzes the hydroalkenylation of aromatic and aliphatic terminal alkynes and enynes with 2‐vinylpyridine to afford 2‐(4R‐butadienyl)pyridines with Z,E configuration as the major reaction products (yield up to 89 %). In addition, unprecedented (Z)‐2‐butadienyl‐5R‐pyridine derivatives have been obtained as minor reaction products (yield up to 21 %) from the elusive 1Z,3gem‐butadienyl hydroalkenylation products. These compounds undergo a thermal 6π‐electrocyclization to afford bicyclic 4H‐quinolizine derivatives that, under catalytic reaction conditions, tautomerize to 6H‐quinolizine to afford the (Z)‐2‐(butadienyl)‐5R‐pyridine by a retro‐electrocyclization reaction