Antifungal and Spectral Studies of Cr(III) and Mn(II) Complexes Derived from <mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML"><mml:mn mathvariant="bold">3</mml:mn><mml:mo>,</mml:mo><mml:msup><mml:mn mathvariant="bold">3</mml:mn><mml:mo>′</mml:mo></mml:msup></mml:math>-Thiodipropionic Acid Derivative : Table 2

]>Antifungal and Spectral Studies of Cr(III) and Mn(II) Complexes Derived from <mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML"><mml:mn mathvariant="bold">3</mml:mn><mml:mo>,</mml:mo><mml:msup><mml:mn mathvariant="bold">3</mml:mn><mml:mo>′</mml:mo></mml:msup></mml:math>-Thiodipropionic Acid Derivative : Table 2

Table 2: Antifungal activity data of the compounds.


Compound	Fungal inhibition (%) (conc. in gm )
	A. brassicae			A. niger			F. oxysporum
	100	200	300	100	200	300	100	200	300

Ligand	40	52	62	35	50	58	42	60	66
Cr(L)NO₃(NO₃)₂	45	58	67	45	56	64	48	68	72
Cr(L)ClCl₂	46	58	66	44	55	63	48	66	74
Cr(L)OAc(OAc)₂	45	59	66	45	56	63	46	66	75
Mn(L)NO₃NO₃	42	56	65	40	54	62	45	62	68
Mn(L)ClCl	44	55	64	38	52	60	45	62	68
Mn(L)OAcOAc	42	55	65	40	54	60	44	63	70
Standard (Captan)	70	80	100	75	90	100	65	75	100