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Publication Date

Thu Mar 30 2023

Journal Name

Iraqi Journal Of Science

Volume

56

Issue Number

3B

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On (m,n) (U,R) – Centralizers

Prime ring

Semiprime ring

Left (right) Centralizer

Left(right) Jordan Centalizer

(m

n)-Jordan Centralizer

Left(righ)(m

n)(U

R)-Centralizer

(m

n)(U

R)-Centalizer

Abdulrahmam

Haneen

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Let m ≥ 1,n ≥ 1 be fixed integers and let R be a prime ring with char (R) ≠2 and
(m+n). Let T be a (m,n)(U,R)-Centralizer where U is a Jordan ideal of R and T(R)
⊆ Z(R) where Z(R) is the center of R ,then T is (U,R)- Centralizer.

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Publication Date

Thu Jan 20 2022

Journal Name

Ibn Al-haitham Journal For Pure And Applied Sciences

Fuzzy Soc-Semi-Prime Sub-Modules

F-module

F-sub-module

F-prime sub-module

Socle of F-module.

Saad S.

Hatam Yahya

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In this paper, we study a new concept of fuzzy sub-module, called fuzzy socle semi-prime sub-module that is a generalization the concept of semi-prime fuzzy sub-module and fuzzy of approximately semi-prime sub-module in the ordinary sense. This leads us to introduce level property which studies the relation between the ordinary and fuzzy sense of approximately semi-prime sub-module. Also, some of its characteristics and notions such as the intersection, image and external direct sum of fuzzy socle semi-prime sub-modules are introduced. Furthermore, the relation between the fuzzy socle semi-prime sub-module and other types of fuzzy sub-module presented.

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Publication Date

Tue Oct 20 2020

Journal Name

Ibn Al-haitham Journal For Pure And Applied Sciences

Approximaitly Quasi-primary Submodules

: Prime submodules

Primary submodules

Socle of modules

Radical of submodules

Multiplication modules

Nonsingular modules.

Ali

Omar

Haibat

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In this paper, we introduce and study the notation of approximaitly quasi-primary submodules of a unitary left -module over a commutative ring with identity. This concept is a generalization of prime and primary submodules, where a proper submodule of an -module is called an approximaitly quasi-primary (for short App-qp) submodule of , if , for , , implies that either or , for some . Many basic properties, examples and characterizations of this concept are introduced.

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Publication Date

Wed Sep 12 2018

Journal Name

Ibn Al-haitham Journal For Pure And Applied Sciences

W-Closed Submodule and Related Concepts

Closed submodules

Weak essential submodules

W-closed submodules

completely essential modules

y-closed submodules

Minimal semi-prime submodules.

Haibat

Mohammad

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Let R be a commutative ring with identity, and M be a left untial module. In this paper we introduce and study the concept w-closed submodules, that is stronger form of the concept of closed submodules, where asubmodule K of a module M is called w-closed in M, "if it has no proper weak essential extension in M", that is if there exists a submodule L of M with K is weak essential submodule of L then K=L. Some basic properties, examples of w-closed submodules are investigated, and some relationships between w-closed submodules and other related modules are studied. Furthermore, modules with chain condition on w-closed submodules are studied.

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Publication Date

Sun Jan 20 2019

Journal Name

Ibn Al-haitham Journal For Pure And Applied Sciences

T-ABSO T-Abso and T-Abso Quasi Primary Fuzzy Submodules

T-ABSO fuzzy ideal

T-ABSO fuzzy submodule

Quasi- prime fuzzy submodule

T-ABSO primary fuzzy submodule

T-ABSO quasi primary fuzzy submodule

Multiplication fuzzy module.

Wafaa H.

Hatem Y.

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Let á¸¾ be a unitary R-module and R is a commutative ring with identity. Our aim in this paper to study the concepts T-ABSO fuzzy ideals, T-ABSO fuzzy submodules and T-ABSO quasi primary fuzzy submodules, also we discuss these concepts in the class of multiplication fuzzy modules and relationships between these concepts. Many new basic properties and characterizations on these concepts are given.

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(1)

Publication Date

Sat Sep 01 2018

Journal Name

Polyhedron

Novel dichloro (bis {2-[1-(4-methylphenyl)-1H-1, 2, 3-triazol-4-yl-κN3] pyridine-κN}) metal (II) coordination compounds of seven transition metals (Mn, Fe, Co, Ni, Cu, Zn and Cd)

The 1

3-dipolar cycloaddition “click” reaction between an azide and an alkyne to give a 1

2

3-triazole was reported by Huisgen in 1961 [1]. In 2002 the Copper(I)-catalyzed Azide-Alkyne Cycloaddition (CuAAC) to prepare a 1

2

3-triazole was reported [2]

[3]. The existence of relatively basic nitrogen atoms in the 1

2

3-triazole rings

and the possibility of introducing additional donor groups in the substituents (Fig. 1)

made the CuAAC “click” reaction an attractive method to prepare differently substituted 1

2

3-triazoles. These compounds have been used as ligands to coordinate to various metal ions that display a range of applications such as in electrochemical and photochemical studies

in supramolecular chemistry

magnetism

metal-ion sensing and catalysis [4]. The reasons for the success of the “click” reaction

is that it is easy to carry out and is widely applicable. It is not affected by a variety of functional groups

and can be carried out with a variety of Cu(I) catalysts and solvents

including aqueous conditions. The Cu(I) catalysts overcome the high activation energy barrier of the non-catalyzed Huisgen reaction by changing the mechanism of the reaction. A large variety of copper catalysts can be used for the CuAAC reaction

on condition that the maximum concentration of Cu(I) species is generated during the reaction. The pre-catalyst can be a Cu(II) salt (usually CuSO4) together with a reducing agent (often sodium ascorbate) or a Cu(I) compound in the presence of a base or amine ligand and a reducing agent to prevent oxidation to Cu(II). Some strong oxidising cupric salts or complexes such as Cu(OAc)2 also work. The solvent is very flexible from organic to aqueous

with the most commonly used combination water + an alcohol (t-BuOH

MeOH or EtOH). The key role of the solvent or solvent mixture is to solubilize the substrates and Cu(I) catalyst in order to ensure rapid reactions. Such aqueous conditions are very useful for biochemical conjugations

as well as for organic syntheses. We recently reported on the synthesis of a series of differently substituted 1

2

3-triazole chromophores

the substituted 2-(1-phenyl-1H-1

2

3-triazol-4-yl)pyridine ligands [5]

see Fig. 2 middle

with substituents R = H (L1)

CH3 (L2)

OCH3 (L3)

COOH

F

Cl

CN

CF3

O(CH2)3CH3 and N(CH3)2. These versatile ligands were found to coordinate to various first row transition metals

such as manganese

cobalt and nickel [6]. Here we extend the series to include more first row transition metal(II) coordination compounds

iron

copper and zinc

as well as a second row transition metal(II) coordination compound

cadmium

containing the 2-(1-(4-methyl-phenyl)-1H-1

2

3-triazol-1-yl)pyridine chromophore (Fig. 2 right with R = CH3). This series of seven novel coordination compounds is the first series of pyridyl-triazole based transition metal coordination compounds where seven different transition metals are coordinated to the same 1

2

3-triazole chromophore

namely 2-(1-(4-methyl-phenyl)-1H-1

2

3-triazol-1-yl)pyridine.

Kinaan M

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