First synthesis and structural determination of 1, 1′‐spirobis(3H‐2, 1‐benzoxatellurole)‐3, 3′‐dione ([10‐Te‐4(C202)])

Yutaka Takaguchi, Naomichi Furukawa

Research output: Contribution to journalArticle

17 Citations (Scopus)

Abstract

1, 1′‐Spirobis(3H‐2, 1‐benzoxatellurole) ‐3, 3′‐dione [10‐Te‐4(C202)] (1c) with five‐membered spirorings was prepared, and its molecular structure was determined by X‐ray crystallographic analysis. The two types of arrangement of the ligands about the central tellurium atom show considerably distorted trigonal bipyramidal (TBP) geometries. The tellurane 1c undergoes a ring‐opening reaction on treatment with aqueous sodium hydroxide to afford the telluroxide 10, which reacts with aqueous hydrochloric acid at room temperature to give again the tellurane 1c in quantitative yield. © 1995 John Wiley & Sons, Inc.

Original languageEnglish
Pages (from-to)481-484
Number of pages4
JournalHeteroatom Chemistry
Volume6
Issue number5
DOIs
Publication statusPublished - 1995
Externally publishedYes

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Tellurium
Sodium Hydroxide
Hydrochloric Acid
Molecular structure
Ligands
Atoms
Geometry
Temperature

ASJC Scopus subject areas

  • Chemistry(all)

Cite this

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title = "First synthesis and structural determination of 1, 1′‐spirobis(3H‐2, 1‐benzoxatellurole)‐3, 3′‐dione ([10‐Te‐4(C202)])",
abstract = "1, 1′‐Spirobis(3H‐2, 1‐benzoxatellurole) ‐3, 3′‐dione [10‐Te‐4(C202)] (1c) with five‐membered spirorings was prepared, and its molecular structure was determined by X‐ray crystallographic analysis. The two types of arrangement of the ligands about the central tellurium atom show considerably distorted trigonal bipyramidal (TBP) geometries. The tellurane 1c undergoes a ring‐opening reaction on treatment with aqueous sodium hydroxide to afford the telluroxide 10, which reacts with aqueous hydrochloric acid at room temperature to give again the tellurane 1c in quantitative yield. {\circledC} 1995 John Wiley & Sons, Inc.",
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T1 - First synthesis and structural determination of 1, 1′‐spirobis(3H‐2, 1‐benzoxatellurole)‐3, 3′‐dione ([10‐Te‐4(C202)])

AU - Takaguchi, Yutaka

AU - Furukawa, Naomichi

PY - 1995

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N2 - 1, 1′‐Spirobis(3H‐2, 1‐benzoxatellurole) ‐3, 3′‐dione [10‐Te‐4(C202)] (1c) with five‐membered spirorings was prepared, and its molecular structure was determined by X‐ray crystallographic analysis. The two types of arrangement of the ligands about the central tellurium atom show considerably distorted trigonal bipyramidal (TBP) geometries. The tellurane 1c undergoes a ring‐opening reaction on treatment with aqueous sodium hydroxide to afford the telluroxide 10, which reacts with aqueous hydrochloric acid at room temperature to give again the tellurane 1c in quantitative yield. © 1995 John Wiley & Sons, Inc.

AB - 1, 1′‐Spirobis(3H‐2, 1‐benzoxatellurole) ‐3, 3′‐dione [10‐Te‐4(C202)] (1c) with five‐membered spirorings was prepared, and its molecular structure was determined by X‐ray crystallographic analysis. The two types of arrangement of the ligands about the central tellurium atom show considerably distorted trigonal bipyramidal (TBP) geometries. The tellurane 1c undergoes a ring‐opening reaction on treatment with aqueous sodium hydroxide to afford the telluroxide 10, which reacts with aqueous hydrochloric acid at room temperature to give again the tellurane 1c in quantitative yield. © 1995 John Wiley & Sons, Inc.

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