Reactivity of vinylidene complexes of ruthenium with hydrazines and hydroxylamines.

نویسندگان

  • Gabriele Albertin
  • Stefano Antoniutti
  • Marco Bortoluzzi
  • Alessandra Botter
  • Jesús Castro
چکیده

Vinylidene complexes [Ru(η(5)-C5H5){[double bond, length as m-dash]C[double bond, length as m-dash]C(H)R}(PPh3)L]BPh4 (, ) [L = P(OMe)3, P(OEt)3; R = Ph, p-tolyl, Bu(t), H] react with hydrazine R1NHNH2 (R1 = H, Me, Ph) to afford nitrile derivatives [Ru(η(5)-C5H5)(N[triple bond, length as m-dash]CCH2R)(PPh3)L]BPh4 (, ) and amine R1NH2. Hydroxylamine NH2OH also reacts with vinylidenes , to yield nitrile derivatives , and H2O. Studies with (15)N-labeled hydrazine and DFT calculations allowed a reaction path to be proposed. The complexes were characterized by spectroscopy (IR, (1)H, (31)P, (13)C and (15)N NMR) and by X-ray crystal structure determination of [Ru(η(5)-C5H5)(N[triple bond, length as m-dash]CCH2Ph)(PPh3){P(OEt)3}]BPh4 ().

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Reactivity of ruthenium vinylidene complexes containing indenyl/dppe ligands and unsaturated bonds at Cδ with trimethylsilyl azide.

This study presents a new reaction of cationic vinylidene complexes with Me₃SiN₃ (TMSN₃), which yields N-coordinated nitrile complexes 3. Treatment of a ruthenium acetylide precursor containing indenyl and dppe ligands with a series of organic halides produced the corresponding vinylidene complexes 2 in good yield. Further reaction of 2 with TMSN₃ at room temperature produced N-coordinated ruth...

متن کامل

Cyclopropenation of organometallic vinylidene complexes

The chemistry of metal cyclopropenyl complexes derived from deprotonation of cationic ruthenium vinylidene complexes is reviewed. Such a metal coordinated cyclopropenyl ligand can be used for the preparation of heterocyclic compounds. The chemical reactivity of cyclopropenyl complexes is influenced by the nature of substituents on the three-membered ring and by the nature of ancillary ligand ar...

متن کامل

Vinylidene rutheniums with an electrostructurally-flexible NO ligand and their ruthenacyclobutene formation.

Vinylidene ruthenium complexes were prepared from trichloronitrosylbis(phosphine)rutheniums and terminal alkynes, subsequent cycloaddition of methyl propiolate to the vinylidene complexes giving rise to unusual ruthenacyclobutene species; in these transformations, an interesting electrostructurally-flexible behaviour of the NO ligand was observed.

متن کامل

Intramolecular Diels-Alder Reactions in Ruthenium Vinylidene Complexes Containing Anthracenyl Groups

An intramolecular Diels-Alder (IMDA) reaction was observed at room temperature between an allyl group and a chloroanthracenyl group that were both bonded to the vinylidene ligand of the cationic ruthenium complex [Ru]dCdC(CH2CHdCH2)CH(CH2CHdCH2)(C14H8Cl) (6; [Ru] ) Cp(PPh3)3Ru). The vinylidene ligand functions as a mediator to bring the allyl and the chloroanthracenyl groups in proximity for th...

متن کامل

Reactions of Ruthenium Acetylide and Vinylidene Complexes Containing a 2-Pyridyl Group

Two ruthenium acetylide complexes [Ru]CtC(C5H3RN) (1a, R ) H; 1b, R ) Me; [Ru] ) Cp(PPh3)2Ru) containing 2-pyridyl groups are prepared and their chemical reactivities are explored. Protonation of the ruthenium acetylide complex 1a with HBF4 takes place at both the nitrogen atom and C , giving the dicationic pyridiniumvinylidene complex {[Ru]dCdC(H)(C5H4NH)}(BF4)2 (3a). Addition of BF3 to 1a yie...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:
  • Dalton transactions

دوره 44 7  شماره 

صفحات  -

تاریخ انتشار 2015