• Korean Journal of Environmental Biology
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• v.21 no.2
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• pp.158-163
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• 2003

This study was conducted te evaluate the effect of organotin compounds on rotifer(Brachionus plicatilis), which is important as food organism of aqua-cultured fish and shellfish. To evaluate the texicities of tributyltin compounds such as tributyltin chloride (TBTC), tributyltin oxide (TBTO), tributyltin acetate (TBTA) and tributyltin benzoate (TBTB), and triphenyltin compounds such as triphenyltin chloride (TPTC), triphenyltin fluoride (TPTF), triphenyltin hydroxide (TPTB), the survival rates of rotifer exposed to these compounds were measured as the 96 hr-$LC_{50}$. Exposed concentrations Were from 0.5 to 8 bbp depending on compounds. Based on 96 hr-$LC_{50}$ Value, the Order of toxicity in TBTs was TBTA(1.1 ppb)>TBTC (2.0)>TBTB (3.3)>TBTO(5.6), and that in TPTs was TPTF (1.0)$\geq$TPTC(1.1)>TPTH(1.6). Triphenyltin compounds were slightly higher toxic than tributyltins. The toxicity is likely to depend on alkyl or aryl group other than halogen or the other substituted radicals.

• Proceedings of the Korean Society of Fisheries Technology Conference
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• 2000.05a
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• pp.373-374
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• 2000

Tributylin(TBT)과 Triphenyltin(TPT) 같은 유기주석화합물은 선박, 어망, 어구등 방오도료의 소재로 사용되어 왔으나 최근 해양생물에게 미치는 독성 때문에 세계 각 국에서도 그 사용을 금지하고 있다. 우리 나라의 경우, 한국 해양연구소가 내분비 교란물질(환경호르몬)의 농도를 조사한 결과 다른 지역에 비해 내만 지역에서의 오염도가 다소 높다고 보고되어 있다. 내만지역의 경우는 파도가 약하여 양식장이 많으므로 양식어류가 TBT와 같은 유기주석 화합물에 노출될 가능성은 매우 높다. (중략)

• Proceedings of the Korean Society of Fisheries Technology Conference
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• 2002.05a
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• pp.494-495
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• 2002

• Proceedings of the Zoological Society Korea Conference
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• 1995.10b
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• pp.156.2-156
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• 1995

• Bulletin of the Korean Chemical Society
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• v.11 no.2
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• pp.164-166
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• 1990

• Proceedings of the Zoological Society Korea Conference
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• 2000.10a
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• pp.186.2-186
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• 2000

No Abstract, See Full Text

• Journal of the korean society of oceanography
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• v.33 no.3
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• pp.90-99
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• 1998

Butyltin and phenyltin residues were quantified in seawater and biota of the Chinhae Bay System, Korea in 1995. Butyltin compounds were detected in all seawater and biota samples, whereas phenyltin compounds were found only in the biota samples. Tributyltin (TBT) concentrations in seawater ranged from < 8-35 ng Sn/l. Tributyltin concentrations in Crassostyea gigas and Thais clavigera ranged from 95-885 and 23-414 ng Sn/g, respectively, Triphenyltin(TPhT) concentrations in each species ranged 155-678 and 46-785 ng Sn/g, respectively. Spatial distribution of TBT was closely related to boating and dry-docking activities. However, spatial distribution of TPhT was not consistent with that of TBT. The biological concentration factor for TBT in C. gigas was about 25000 that is four times greater than that of T. clavigera. Butyl- to phenyltin concentration ratio was greater than one in C. gigas, but that in T. clavigera was less than one. Major tissues of C. gigas also showed different accumulation patterns for butyl- and phenyltin compounds. Furthermore, 19 and 28% of total body burdens of TBT and TPhT were found in gonadal mass of C. gigas just prior to spawning.

• Journal of the Korean Chemical Society
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• v.31 no.1
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• pp.79-83
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• 1987

Trimethyl-and triphenyl-metal (IVA) methoxides were reacted with phenylisocyanate at various temperatures. Even at 100$^{\circ}C$, methyltrimethylsilyl ether, methyltriphenylsilyl ether and triphenyltin methoxide produced the cyclic dimer of phenylisocyanate, N,N'-diphenyluretidine-2,4-dione. But the other compounds produced only the cyclic trimer of phenylisocyanate, phenylisocyanurate. And above 200$^{\circ}C$, considerable amounts of diphenylcarbodiimide was formed by all the organometallic compounds. From these results, the mechanism of cyclic polymerization of phenylisocyanate by the organometal catalysts, and the correlation of substituents with the reactivity were discussed.

• 대한생식의학회:학술대회논문집
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• 2005.06a
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• pp.114-114
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• 2005

• Archives of Pharmacal Research
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• v.12 no.3
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• pp.231-232
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• 1989

Although it has been known that organometallic $\beta$-lactam compounds improve the resistance to $\beta$-lactamases as well as their pharmacological activities, only a few results on organometallic $\beta$-lactam antibiotics were reported. In the course of our extensive study on the development of new cephalosporins, we were interested in organotin compounds since they show some biological activities.