Journals / Turkish Journal of Chemistry / 2005 / Cilt: 29 - Sayı: 5

Organotin(IV) Derivatives of N-Maleoylamino Acids: Their Synthesis and Structural Elucidation

Pages
463–476
Publication Date
2005-05-01
DOI
—
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

Salient features of the X-ray structures for (1), (4) and (6) are also given.

📌 3 Key Takeaways

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Objective & Hypothesis:Organotin carboxylates of general formula R3SnL (1), (2), (4) and (6), R2SnL2 (5) and {[(R2SnL)2O]2} (3), where L = N-maleoylglycinate, N-maleoyl-b-alaninate and N-maleoylmethioninate, were prepared.
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Key Findings & Data:The synthesis of these compounds was achieved by either reaction of organotin halides, R3SnCl, with triethylammonium salt of N-maleoylamino acids or/and organotin oxides, (R3Sn)2O and R2SnO, with maleamic acid in the presence of triethyl amine.
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Conclusion & Impact:Salient features of the X-ray structures for (1), (4) and (6) are also given.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Organotin(IV) complexes · N-Maleoylamino acids · FT-IR

Abstract

Organotin carboxylates of general formula R3SnL (1), (2), (4) and (6), R2SnL2 (5) and {[(R2SnL)2O]2} (3), where L = N-maleoylglycinate, N-maleoyl-b-alaninate and N-maleoylmethioninate, were prepared. The synthesis of these compounds was achieved by either reaction of organotin halides, R3SnCl, with triethylammonium salt of N-maleoylamino acids or/and organotin oxides, (R3Sn)2O and R2SnO, with maleamic acid in the presence of triethyl amine. These compounds were characterized by FT-IR, multinuclear NMR (1H, 13C and 119Sn), mass and 119mSn Mössbauer spectroscopy. The geometry around the tin atom is compared both in solution and in solid state. Different literature methods were employed to calculate the C-Sn-C angle in non-coordinating solvents. The mass fragmentation pattern demonstrated the McLafferty rearrangement in compound (6). Salient features of the X-ray structures for (1), (4) and (6) are also given.

Özet

Organotin carboxylates of general formula R3SnL (1), (2), (4) and (6), R2SnL2 (5) and {[(R2SnL)2O]2} (3), where L = N-maleoylglycinate, N-maleoyl-b-alaninate and N-maleoylmethioninate, were prepared. The synthesis of these compounds was achieved by either reaction of organotin halides, R3SnCl, with triethylammonium salt of N-maleoylamino acids or/and organotin oxides, (R3Sn)2O and R2SnO, with maleamic acid in the presence of triethyl amine. These compounds were characterized by FT-IR, multinuclear NMR (1H, 13C and 119Sn), mass and 119mSn Mössbauer spectroscopy. The geometry around the tin atom is compared both in solution and in solid state. Different literature methods were employed to calculate the C-Sn-C angle in non-coordinating solvents. The mass fragmentation pattern demonstrated the McLafferty rearrangement in compound (6). Salient features of the X-ray structures for (1), (4) and (6) are also given.

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Cite This Article

BHATTI, M. H., ALI, S., HUMA, F. (2005). Organotin(IV) Derivatives of N-Maleoylamino Acids: Their Synthesis and Structural Elucidation. Turkish Journal of Chemistry, Cilt: 29 - Sayı: 5, 463–476. https://ajindex.com/articles/227810

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