AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
The chloroarsinidene compound Cp'(CO)2Mn-As(Cl)-Mn(CO)2Cp', 1a, (Cp' = eta-5-C5H4CH3) upon reaction with GaCl3 transforms into the tetrachlorogallate of the dimanganaarsacumuleniumion [Cp'(CO)2Mn = As = Mn(CO)2Cp']+, 2a. The cumulene type bonding in 2a is evidenced by the spectroscopic and structural (X-ray analysis of 2a.GaCl4-) properties. The chloroarsinidene compound (CO)5Cr-As(Cl)-Cr(CO)5, 1b, and the chlorostibinidene complex Cp-star-(CO)2Mn-Sb(Cl)-Mn(CO)2-Cp-star, 1c, (Cp-star = eta-5-C5(CH3)5) are correspondingly transformed into dimetallaarsa- ([(CO)5Cr = As = Cr(CO)5]+, 2b) and dimetallastiba- ([Cp-star-(CO)2Mn = Sb = Mn(CO)2Cp-star]+, 2c) cumuleniumions respectively. The cations 2b, 2c are unequivocally characterized by spectroscopic techniques; however, crystal structure analyses could not yet be obtained.Under similar conditions the chlorostibinidene compound Cp'(CO)2Mn-Sb(Cl)-Mn(CO)2Cp', 1d, gives the trinuclear cation [Cp'(CO)2 activative Mn]-Cp'(CO)2Mn-Sb = Mn(CO)2Cp'+, 4, which, as shown by X-ray analysis of 4.CF3SO3-, contains a trigonally planar coordinated Sb+-cation.
The dimetallaarsacumuleniumion [Cp'(CO)2Mn = As = Mn(CO)2Cp']+, 2, which is easily obtained by halide abstraction from the arsinidene complex Cp'(CO)2Mn-As-(Cl)-Mn(CO)2Cp', 1a, reacts with nucleophiles X- to give the arsinidene species Cp'(CO)2Mn-As(X)-Mn(CO)2Cp', 1c-1f (1c: X = 1, 1d: X = NCO, 1e: X = NCS, 1f: X = N3); with BH4- as the nucleophile the parent compound Cp'(CO)2Mn-As(H)-Mn(CO)2Cp', 1b, is obtained.The new arsinidene compounds 1b-1f are characterized by the standard analytic and spectroscopic techniques; in addition X-ray analyses are reported for 1b, 1c and 1e.
The dimetallaarsacumuleniumion [Cp′(CO)2MnAsMn(CO)2Cp′]+, 2, (Cp′ = η5-C5H4CH3) obtained from the arsinidene compound , 1a, reacts with dipy to give the cationic arsenic(I) chelate compound [Cp′(CO)2Mn]2 As[dipy]+, which has been isolated and structurally characterized as its CF3SO3− salt, 3a. ortho-Phenanthroline as the chelate ligand gives the corresponding o-phen chelate, isolated as its triflate 3b.
AbstractTitle ions such as in (II) (space group P1, Z=2) are prepared by halide abstraction from the arsinidene compound (I).
AbstractDer Arsinidenkomplex [Cp′(CO)2Mn]2AsCl, 1, (Cp′ C5H4CH3) reagiert mit TIPF6 zunächst unter Bildung eines Salzes von [Cp′(CO)2MnAsMn(CO)2Cp′]+, das bei längerer Reaktionszeit in den Fluorarsinidenkomplex [Cp′(CO)2Mn]2AsF, 3, übergeht. Einfacher wird 3 aus 1 und TIF erhalten.Die Struktur des Salzes [Cp′(CO)2MnAsMn(CO)2Cp]+CF3SO3−, 2, das aus Chloridabstraktion aus 1 erhalten worden war, wird diskutiert. Einen Zugang zu Komplexen 5 mit dem [CP*(CO)2MnAsMn(CO)2Cp*]+‐Kation (Cp* C5(CH3)5) bietet die Hydridabstraktion aus [Cp*(CO)2Mn]2AsH, 4, mit den Carbenium‐Ion‐Äquivalenten Et3OBF4, Ph3CPF6 und CF3SO3CH3 sowie mit den Säuren CF3SO3H und H2SO4.
ChemInformVolume 20, Issue 16 Organoelement Compounds ChemInform Abstract: ((Cp*(CO)2Mn)2P)+ X- (X = CF3SO3, PF6; Cp* = C5Me5), the First Dimetallaphosphacumulenes. A. STRUBE, A. STRUBE Anorg. Chem. Inst., Univ., D-6900 HeidelbergSearch for more papers by this authorJ. HEUSER, J. HEUSER Anorg. Chem. Inst., Univ., D-6900 HeidelbergSearch for more papers by this authorG. HUTTNER, G. HUTTNER Anorg. Chem. Inst., Univ., D-6900 HeidelbergSearch for more papers by this authorH. LANG, H. LANG Anorg. Chem. Inst., Univ., D-6900 HeidelbergSearch for more papers by this author A. STRUBE, A. STRUBE Anorg. Chem. Inst., Univ., D-6900 HeidelbergSearch for more papers by this authorJ. HEUSER, J. HEUSER Anorg. Chem. Inst., Univ., D-6900 HeidelbergSearch for more papers by this authorG. HUTTNER, G. HUTTNER Anorg. Chem. Inst., Univ., D-6900 HeidelbergSearch for more papers by this authorH. LANG, H. LANG Anorg. Chem. Inst., Univ., D-6900 HeidelbergSearch for more papers by this author First published: April 18, 1989 https://doi.org/10.1002/chin.198916282Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onFacebookTwitterLinked InRedditWechat No abstract is available for this article. Volume20, Issue16April 18, 1989 RelatedInformation
The organometallic cumulenes, [Cp*(CO)2MnPMn(CO)2Cp*]+X− (3: X CF3SO3, PF6; Cp* C5Me5) have been obtained by hydride abstraction from [Cp*(CO)2Mn]2PH (2). They are the first phosphorus analogues of the recently synthesized arsenic compounds [Cp*(CO)2MNAsMn(CO)2Cp*]+X−.
AbstractThe water‐sensitive title complex (IIa) is obtained according to the scheme and characterized by IR, 1H NMR, and UV spectral data.