<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE ArticleSet PUBLIC "-//NLM//DTD PubMed 2.7//EN" "https://dtd.nlm.nih.gov/ncbi/pubmed/in/PubMed.dtd">
<ArticleSet>
<Article>
<Journal>
				<PublisherName>University of Tehran</PublisherName>
				<JournalTitle>Journal of Sciences, Islamic Republic of Iran</JournalTitle>
				<Issn>1016-1104</Issn>
				<Volume>6</Volume>
				<Issue>2</Issue>
				<PubDate PubStatus="epublish">
					<Year>1995</Year>
					<Month>06</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>ISOLATION AND CHARACTERIZATION OF SIX
HIGHLY INTRINSIC FLUORESCENT
METABOLITES IN ARMILLARIA MELLEA
(VAHL. EX. FR.) KARST</ArticleTitle>
<VernacularTitle>-</VernacularTitle>
			<FirstPage></FirstPage>
			<LastPage></LastPage>
			<ELocationID EIdType="pii">31410</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
		<Abstract>Six fluorescent compounds were isolated and characterized in rhizomorph of
A. mellea and were presented first as: F , F , F , MF , MF  and MF . These
compounds differed by Rf on chromatoplaque,  max in UV spectra and  ex,
 em and  max in fluorescence spectra. Their GC-MS analysis indicated that F 
has a phenolic moiety and the other five are the benzenic derivatives. F 
compound was more fluorescent resulting from its hydroxyl group. The
difference between the fluorescent compounds of rhizomorph and hyphae
suggests the participation of some of these compounds in differentiation.
Moreover, these compounds may have antibiotic activity against their hosts or
enemies</Abstract>
<ArchiveCopySource DocType="pdf">https://jsciences.ut.ac.ir/article_31410_5994cf5ebd61f4806932d5f226cb64d0.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>University of Tehran</PublisherName>
				<JournalTitle>Journal of Sciences, Islamic Republic of Iran</JournalTitle>
				<Issn>1016-1104</Issn>
				<Volume>6</Volume>
				<Issue>2</Issue>
				<PubDate PubStatus="epublish">
					<Year>1995</Year>
					<Month>06</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>TERATOGENIC EFFECTS OF LITHIUM
CARBONATE ON DEVELOPMENT OF MOUSE
EMBRYOS</ArticleTitle>
<VernacularTitle>-</VernacularTitle>
			<FirstPage></FirstPage>
			<LastPage></LastPage>
			<ELocationID EIdType="pii">31411</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
		<Abstract></Abstract>
<ArchiveCopySource DocType="pdf">https://jsciences.ut.ac.ir/article_31411_e4b976d55a102a5b6ff224fef96b74d1.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>University of Tehran</PublisherName>
				<JournalTitle>Journal of Sciences, Islamic Republic of Iran</JournalTitle>
				<Issn>1016-1104</Issn>
				<Volume>6</Volume>
				<Issue>2</Issue>
				<PubDate PubStatus="epublish">
					<Year>1995</Year>
					<Month>06</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>LEWIS BASE ADDUCTS OF LEAD(I1)
COMPOUNDS 111*
SYNTHESIS AND STRUCTURAL
CHARACTERIZATION OF
LPb(C10,), AND LPb(NCS),,
(L= MESO-5,7,7,12,14, 14-HEXAMETHYL- 1,4,8,11-
TETRA-AZACY COTETRADECANE)</ArticleTitle>
<VernacularTitle>-</VernacularTitle>
			<FirstPage></FirstPage>
			<LastPage></LastPage>
			<ELocationID EIdType="pii">31412</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
		<Abstract>The reactions of Pb(C10 ) , and Pb(SCN)  with meso-5,7,7,12,14,14-hexamethyl-
1,4,8,ll ,tetra-azacyclotetradecane (C ,H ,N = L) yielded colorless crystals of
LPb(CI O  ) (1) and LPb(NCS)  (2), respectively. Their structures were determined
by X-ray crystallography. Crystal data: 1 monoclinic, P 2 /c, a =11.293 (4) ?,
b = 16.382 (6) ? , c = 21.518(4) ?, ? = 92.14(2)?, Z = 4, MoKa, 1824 observed
(1&gt;2.5?(I )) data (20°C), R = 0.044; 2 ,orthorombic, P cab, a = 15.861(2) ? ,
b = 10.436(8) ?, c = 20.347(4) ?, ? = 90.00(3)?, Z= 4, MoK?, 1763 observed
(1&gt;2.5?(I) data (20°C), R= 0.05 1. In both molecules, lead(II) cation is situated above
the plane of the macrocyclic ring</Abstract>
<ArchiveCopySource DocType="pdf">https://jsciences.ut.ac.ir/article_31412_63d01849974fcec145c71b5ebb80e184.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>University of Tehran</PublisherName>
				<JournalTitle>Journal of Sciences, Islamic Republic of Iran</JournalTitle>
				<Issn>1016-1104</Issn>
				<Volume>6</Volume>
				<Issue>2</Issue>
				<PubDate PubStatus="epublish">
					<Year>1995</Year>
					<Month>06</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>SYNTHESIS  OF SELENAZOL0[3,2-b] [ 1,2,4]
TRIAZINE AND SELENAZOLO [2,3-C] [I ,2,4]
TRIAZINE</ArticleTitle>
<VernacularTitle>-</VernacularTitle>
			<FirstPage></FirstPage>
			<LastPage></LastPage>
			<ELocationID EIdType="pii">31413</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
		<Abstract>6-Methyl- 1,2,4-triazine-3-(2H)-selenone-5(4H)-one(l) reacts in the presence of
base with phenacyl bromide to give a mixture of compounds (2) and (3). This mixture is dehydrated in the presence of H,SO, to give 3-phenyl-6 methyl-7H-selenazolo[3,2-b] [I ,2,4] triazin-7-one (6). For careful structure assignment of (6) its regioisomer 3-methyl-6-phenyl-4H-selenazolo [2,3-c] [ 1,2,4] triazin-4-one (8) was unambiguously synthesized and its spectroscopic data were Compared with those of (6)</Abstract>
<ArchiveCopySource DocType="pdf">https://jsciences.ut.ac.ir/article_31413_e80a24f4b7d064f350d065d0a5c51123.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>University of Tehran</PublisherName>
				<JournalTitle>Journal of Sciences, Islamic Republic of Iran</JournalTitle>
				<Issn>1016-1104</Issn>
				<Volume>6</Volume>
				<Issue>2</Issue>
				<PubDate PubStatus="epublish">
					<Year>1995</Year>
					<Month>06</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>PREPARATION OF (CHLOROCARBONYL)
PHENYLKETENB AND ITS CYCLOADDITION
REACTION WITH BENZALDEHYDEV</ArticleTitle>
<VernacularTitle>-</VernacularTitle>
			<FirstPage></FirstPage>
			<LastPage></LastPage>
			<ELocationID EIdType="pii">31414</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
		<Abstract>Meldrum&#039;s acid, 2&#039;5-diphenyl-1&#039;3-dioxane-4&#039;6-dione, was produced by [2+2]
cycloadditions of the (chlorocarbony1)phenylketene with benzaldehyde. Acid
hydrolysis of the meldrum&#039;s acid regenerated benzaldehyde and also yielded
phenylacetic acid as the final product</Abstract>
<ArchiveCopySource DocType="pdf">https://jsciences.ut.ac.ir/article_31414_4d83f681638e40203e88cb7cb014b74f.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>University of Tehran</PublisherName>
				<JournalTitle>Journal of Sciences, Islamic Republic of Iran</JournalTitle>
				<Issn>1016-1104</Issn>
				<Volume>6</Volume>
				<Issue>2</Issue>
				<PubDate PubStatus="epublish">
					<Year>1995</Year>
					<Month>06</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>THE EXTENDED LAW OF CORRESPONDING -
STATES AND THE INTERMOLECULAR
POTENTIALS FOR Ar-Ar, Ar-Kr AND Kr-Kr</ArticleTitle>
<VernacularTitle>-</VernacularTitle>
			<FirstPage></FirstPage>
			<LastPage></LastPage>
			<ELocationID EIdType="pii">31415</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
		<Abstract>An inversion procedure is used to obtain from the extended principle of
corresponding - states the pair interaction potentials for argon, krypton and its
mixture over a tetnperature range from absolute zero to the onset of ionization.
The experimentally-reduced viscosity collision integrals obtained from the
corresponding - states correlation have been inverted directly to give the
reduced-intermolecular potential energy curves corresponding to the collision
integrals. These directly determined potentials are in good agreement with the
potentials independently obtained from the molecular-beam scattering
measurements, which were fitted by ESMSV for Ar-Ar and Kr-Kr and by
SMSV for Ar-Kr</Abstract>
<ArchiveCopySource DocType="pdf">https://jsciences.ut.ac.ir/article_31415_fd80c4b06025c38f9d6958ebe4f14532.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>University of Tehran</PublisherName>
				<JournalTitle>Journal of Sciences, Islamic Republic of Iran</JournalTitle>
				<Issn>1016-1104</Issn>
				<Volume>6</Volume>
				<Issue>2</Issue>
				<PubDate PubStatus="epublish">
					<Year>1995</Year>
					<Month>06</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>THE DERIVED GROUP OF A SEIFERT FIBRE
GROUP</ArticleTitle>
<VernacularTitle>-</VernacularTitle>
			<FirstPage></FirstPage>
			<LastPage></LastPage>
			<ELocationID EIdType="pii">31416</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
		<Abstract>Every Seifert Fibre Group is the lift of a Fuchsian group to the universal
covering group of PSL (2,R). From this, we work out a form of presentation for
such a group. With the calculation of the Euler number, we can establish the
presentation of the derived group of a Seifert Fibre Group</Abstract>
<ArchiveCopySource DocType="pdf">https://jsciences.ut.ac.ir/article_31416_d80c2e64d4eaec667e3a3e05d935fe8c.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>University of Tehran</PublisherName>
				<JournalTitle>Journal of Sciences, Islamic Republic of Iran</JournalTitle>
				<Issn>1016-1104</Issn>
				<Volume>6</Volume>
				<Issue>2</Issue>
				<PubDate PubStatus="epublish">
					<Year>1995</Year>
					<Month>06</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>THE ANALOGUE OF WEIGHTED GROUP
ALGEBRA FOR SEMITOPOLOGICAL
SEMIGROUPS</ArticleTitle>
<VernacularTitle>-</VernacularTitle>
			<FirstPage></FirstPage>
			<LastPage></LastPage>
			<ELocationID EIdType="pii">31417</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
		<Abstract>In [1,2,3], A. C. Baker and J.W. Baker studied the subspace Ma(S) of the
convolution measure algebra M, (S) of a locally compact semigroup. H.
Dzinotyiweyi in [5,7] considers an analogous measure space on a large class
of C-distinguished topological semigroups containing all completely regular
topological semigroups. In this paper, we extend the definitions to study the
weighted semigroup algebra Ma (S, o), where o is a weight function on a Cdistinguished
semitopological semigroup S. We will show that this subspace
is a convolution measure algebra. As acorollary, this answers in the affirmative
a question raised by J.W. Baker and H. Dzinotyiweyi in [6]</Abstract>
<ArchiveCopySource DocType="pdf">https://jsciences.ut.ac.ir/article_31417_a9dcc146714bd053238b84413ef7a3ff.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>University of Tehran</PublisherName>
				<JournalTitle>Journal of Sciences, Islamic Republic of Iran</JournalTitle>
				<Issn>1016-1104</Issn>
				<Volume>6</Volume>
				<Issue>2</Issue>
				<PubDate PubStatus="epublish">
					<Year>1995</Year>
					<Month>06</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>VISCOSITY COEFFICIENTS OF THE
A-PHASE OF SUPERFLUID He AT LOW
TEMPERATURES</ArticleTitle>
<VernacularTitle>-</VernacularTitle>
			<FirstPage></FirstPage>
			<LastPage></LastPage>
			<ELocationID EIdType="pii">31418</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
		<Abstract>It has been shown that the Boltzmann equation for the viscosity of the A-phase of
superfluid 3He at low temperatures has the same form as for a normal Ferrni liquid.
The viscosity coefficients A, B, C, D and E are derived exactly. The h , parameter
plays an important role in determining the temperature dependence of the viscosity
coefficients</Abstract>
<ArchiveCopySource DocType="pdf">https://jsciences.ut.ac.ir/article_31418_c219b83bdbd3fc9bf4fa8526d4368ea1.pdf</ArchiveCopySource>
</Article>
</ArticleSet>
