JP2000164608A - Resin-sealed semiconductor device - Google Patents

Resin-sealed semiconductor device

Info

Publication number
JP2000164608A
JP2000164608A JP33355398A JP33355398A JP2000164608A JP 2000164608 A JP2000164608 A JP 2000164608A JP 33355398 A JP33355398 A JP 33355398A JP 33355398 A JP33355398 A JP 33355398A JP 2000164608 A JP2000164608 A JP 2000164608A
Authority
JP
Japan
Prior art keywords
semiconductor chip
semiconductor device
embedded image
resin composition
resin
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP33355398A
Other languages
Japanese (ja)
Other versions
JP3313331B2 (en
Inventor
Takashi Hirano
孝 平野
Toshio Banba
敏夫 番場
Hiroaki Makabe
裕明 真壁
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Sumitomo Bakelite Co Ltd
Original Assignee
Sumitomo Bakelite Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Sumitomo Bakelite Co Ltd filed Critical Sumitomo Bakelite Co Ltd
Priority to JP33355398A priority Critical patent/JP3313331B2/en
Publication of JP2000164608A publication Critical patent/JP2000164608A/en
Application granted granted Critical
Publication of JP3313331B2 publication Critical patent/JP3313331B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Classifications

    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L2224/00Indexing scheme for arrangements for connecting or disconnecting semiconductor or solid-state bodies and methods related thereto as covered by H01L24/00
    • H01L2224/01Means for bonding being attached to, or being formed on, the surface to be connected, e.g. chip-to-package, die-attach, "first-level" interconnects; Manufacturing methods related thereto
    • H01L2224/26Layer connectors, e.g. plate connectors, solder or adhesive layers; Manufacturing methods related thereto
    • H01L2224/31Structure, shape, material or disposition of the layer connectors after the connecting process
    • H01L2224/32Structure, shape, material or disposition of the layer connectors after the connecting process of an individual layer connector
    • H01L2224/321Disposition
    • H01L2224/32151Disposition the layer connector connecting between a semiconductor or solid-state body and an item not being a semiconductor or solid-state body, e.g. chip-to-substrate, chip-to-passive
    • H01L2224/32221Disposition the layer connector connecting between a semiconductor or solid-state body and an item not being a semiconductor or solid-state body, e.g. chip-to-substrate, chip-to-passive the body and the item being stacked
    • H01L2224/32245Disposition the layer connector connecting between a semiconductor or solid-state body and an item not being a semiconductor or solid-state body, e.g. chip-to-substrate, chip-to-passive the body and the item being stacked the item being metallic
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L2224/00Indexing scheme for arrangements for connecting or disconnecting semiconductor or solid-state bodies and methods related thereto as covered by H01L24/00
    • H01L2224/01Means for bonding being attached to, or being formed on, the surface to be connected, e.g. chip-to-package, die-attach, "first-level" interconnects; Manufacturing methods related thereto
    • H01L2224/42Wire connectors; Manufacturing methods related thereto
    • H01L2224/44Structure, shape, material or disposition of the wire connectors prior to the connecting process
    • H01L2224/45Structure, shape, material or disposition of the wire connectors prior to the connecting process of an individual wire connector
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L2224/00Indexing scheme for arrangements for connecting or disconnecting semiconductor or solid-state bodies and methods related thereto as covered by H01L24/00
    • H01L2224/01Means for bonding being attached to, or being formed on, the surface to be connected, e.g. chip-to-package, die-attach, "first-level" interconnects; Manufacturing methods related thereto
    • H01L2224/42Wire connectors; Manufacturing methods related thereto
    • H01L2224/44Structure, shape, material or disposition of the wire connectors prior to the connecting process
    • H01L2224/45Structure, shape, material or disposition of the wire connectors prior to the connecting process of an individual wire connector
    • H01L2224/45001Core members of the connector
    • H01L2224/45099Material
    • H01L2224/451Material with a principal constituent of the material being a metal or a metalloid, e.g. boron (B), silicon (Si), germanium (Ge), arsenic (As), antimony (Sb), tellurium (Te) and polonium (Po), and alloys thereof
    • H01L2224/45138Material with a principal constituent of the material being a metal or a metalloid, e.g. boron (B), silicon (Si), germanium (Ge), arsenic (As), antimony (Sb), tellurium (Te) and polonium (Po), and alloys thereof the principal constituent melting at a temperature of greater than or equal to 950°C and less than 1550°C
    • H01L2224/45144Gold (Au) as principal constituent
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L2224/00Indexing scheme for arrangements for connecting or disconnecting semiconductor or solid-state bodies and methods related thereto as covered by H01L24/00
    • H01L2224/01Means for bonding being attached to, or being formed on, the surface to be connected, e.g. chip-to-package, die-attach, "first-level" interconnects; Manufacturing methods related thereto
    • H01L2224/42Wire connectors; Manufacturing methods related thereto
    • H01L2224/47Structure, shape, material or disposition of the wire connectors after the connecting process
    • H01L2224/48Structure, shape, material or disposition of the wire connectors after the connecting process of an individual wire connector
    • H01L2224/4805Shape
    • H01L2224/4809Loop shape
    • H01L2224/48091Arched
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L2224/00Indexing scheme for arrangements for connecting or disconnecting semiconductor or solid-state bodies and methods related thereto as covered by H01L24/00
    • H01L2224/01Means for bonding being attached to, or being formed on, the surface to be connected, e.g. chip-to-package, die-attach, "first-level" interconnects; Manufacturing methods related thereto
    • H01L2224/42Wire connectors; Manufacturing methods related thereto
    • H01L2224/47Structure, shape, material or disposition of the wire connectors after the connecting process
    • H01L2224/48Structure, shape, material or disposition of the wire connectors after the connecting process of an individual wire connector
    • H01L2224/481Disposition
    • H01L2224/48151Connecting between a semiconductor or solid-state body and an item not being a semiconductor or solid-state body, e.g. chip-to-substrate, chip-to-passive
    • H01L2224/48221Connecting between a semiconductor or solid-state body and an item not being a semiconductor or solid-state body, e.g. chip-to-substrate, chip-to-passive the body and the item being stacked
    • H01L2224/48245Connecting between a semiconductor or solid-state body and an item not being a semiconductor or solid-state body, e.g. chip-to-substrate, chip-to-passive the body and the item being stacked the item being metallic
    • H01L2224/4826Connecting between the body and an opposite side of the item with respect to the body
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L2224/00Indexing scheme for arrangements for connecting or disconnecting semiconductor or solid-state bodies and methods related thereto as covered by H01L24/00
    • H01L2224/73Means for bonding being of different types provided for in two or more of groups H01L2224/10, H01L2224/18, H01L2224/26, H01L2224/34, H01L2224/42, H01L2224/50, H01L2224/63, H01L2224/71
    • H01L2224/732Location after the connecting process
    • H01L2224/73201Location after the connecting process on the same surface
    • H01L2224/73215Layer and wire connectors
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L2924/00Indexing scheme for arrangements or methods for connecting or disconnecting semiconductor or solid-state bodies as covered by H01L24/00
    • H01L2924/10Details of semiconductor or other solid state devices to be connected
    • H01L2924/102Material of the semiconductor or solid state bodies
    • H01L2924/1025Semiconducting materials
    • H01L2924/10251Elemental semiconductors, i.e. Group IV
    • H01L2924/10253Silicon [Si]

Abstract

PROBLEM TO BE SOLVED: To markedly lessen operation man-hours required for manufacturing a resin-sealed semiconductor device by a method wherein inner leads are bonded to a semiconductor chip through the intermediary of a specific coat layer, then the inner leads are connected to the semiconductor chip with bonding wires, and the chip and the bonding wires are sealed up with sealing resin. SOLUTION: A coat layer 1 of positive-type photosensitive resin composition composed of 100 pts.wt. polyamide represented by a formula and 1 to 100 pts.wt. photosensitive diazo quinone compound is provided on the circuit element forming surface of a semiconductor chip 2. The coat layer 1 is made to serve as an adhesive agent, the inner leads of a lead frame 3 are bonded to the semiconductor chip 2, the inner leads are connected to the semiconductor chip 2 with bonding wires 4, and the semiconductor chip 2 and the other components are sealed up with sealing resin 5. In a formula, X denotes a tetravalent cyclic compound group, Y denotes a bivalent cyclic compound group, E is an aliphatic or a cyclic compound group possessed of an alkenyl group, a and b denote a molar fraction, a + b = 100 mol%, R1 and R2 are each a bivalent organic group, and R3 and R4 are each a monovalent organic group.

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】本発明は、高感度で高残膜率
のパターンを得ることがでるポジ型感光性樹脂組成物と
それを用いたリードオンチップ(Lead On Ch
ip)構造を有する半導体装置に関するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a positive photosensitive resin composition capable of obtaining a pattern with high sensitivity and a high residual film ratio, and a lead-on-chip (Lead On Ch) using the same.
The present invention relates to a semiconductor device having an ip) structure.

【0002】[0002]

【従来の技術】半導体素子の大型化に伴い、半導体素子
の回路素子表面形成面上に、両面に接着剤を塗布した絶
縁フィルムを介して複数のインナーリードが前記接着剤
で接着され、該インナーリードと前記半導体素子とがボ
ンディングワイヤで接続され、封止樹脂で封止されたリ
ードオンチップ(Lead On Chip=以下LO
Cという)構造の半導体装置(特公昭61−21813
9号公報)が提案された。しかしながら、樹脂封止型半
導体装置では、予め両面に接着剤を塗布した絶縁フィル
ムを準備し、まずリードフレームに該絶縁フィルムを接
着後、片方の面の接着剤を用いて半導体素子を接着する
ため作業性が悪いという問題があった。更に通常絶縁フ
ィルムとしては、ポリイミド系が用いられるが、ポリイ
ミドフィルムは吸水性が高く、吸湿した水分が半田リフ
ロー時にパッケージの中で気化膨張して、パッケージに
クラックを発生するという問題があった。
2. Description of the Related Art With an increase in the size of a semiconductor element, a plurality of inner leads are adhered to the circuit element surface forming surface of the semiconductor element via an insulating film coated with an adhesive on both sides with the adhesive. The lead and the semiconductor element are connected by a bonding wire, and a lead-on-chip (Lead On Chip = hereinafter LO)
C) semiconductor device (Japanese Patent Publication No. 61-21813)
No. 9) has been proposed. However, in a resin-encapsulated semiconductor device, an insulating film is prepared in which an adhesive is applied to both surfaces in advance, and the insulating film is first adhered to a lead frame, and then the semiconductor element is adhered using the adhesive on one surface. There was a problem that workability was poor. Further, a polyimide film is usually used as the insulating film. However, the polyimide film has a high water absorption, and there is a problem in that the absorbed moisture vaporizes and expands in the package at the time of solder reflow, thereby causing cracks in the package.

【0003】また、特開平6−37243には上記の問
題を解決するための方法が提案されている。これを用い
ると半導体素子作成工程の一部が簡略化でき、工程短縮
および歩留まり向上の効果はあるが、現像の際にN−メ
チル−2−ピロリドン等の溶剤が必要となるため、安全
性、取扱い性に問題がある。
[0003] Japanese Patent Application Laid-Open No. Hei 6-37243 proposes a method for solving the above problem. When this is used, a part of the semiconductor element manufacturing process can be simplified, and there is an effect of shortening the process and improving the yield. However, since a solvent such as N-methyl-2-pyrrolidone is required for development, safety, There is a problem in handling.

【0004】[0004]

【発明が解決しようとする課題】本発明は、前述したL
OC構造を有する封止樹脂半導体装置の製造時の作業性
の欠点を改善し、かつ各種の信頼性に優れた半導体装置
を提供するものである。
SUMMARY OF THE INVENTION The present invention relates to the aforementioned L
An object of the present invention is to provide a semiconductor device having improved workability during production of a sealing resin semiconductor device having an OC structure and having various reliability.

【0005】[0005]

【課題を解決するための手段】本発明は、一般式(I)
で示されるポリアミド100重量部と感光性ジアゾキノ
ン化合物1〜100重量部とからなるポジ型感光性樹脂
組成物のコート層を半導体チップの回路素子形成面上に
有し、該コート層を接着剤とし、複数のインナーリード
を前記半導体チップと接着し、該インナーリードと半導
体チップとが、ボンディングワイヤで接続され、封止樹
脂で封止されたリードオンチップ(Lead On C
hip)構造を有することを特徴とする樹脂封止型半導
体装置であり、また、ポジ型感光性樹脂組成物に一般式
(II)で表わされるビスフェノール化合物および一般式
(III)で表わされるトリスフェノール化合物を、両者
合計1〜30重量部配合してなるポジ型感光性樹脂組成
物を用いる前記の半導体装置である。
The present invention provides a compound represented by the general formula (I):
Having a coating layer of a positive photosensitive resin composition comprising 100 parts by weight of a polyamide and 1 to 100 parts by weight of a photosensitive diazoquinone compound on a circuit element forming surface of a semiconductor chip, and using the coating layer as an adhesive. A plurality of inner leads are adhered to the semiconductor chip, and the inner leads and the semiconductor chip are connected by bonding wires and sealed with a sealing resin (Lead On C).
(b) a resin-encapsulated semiconductor device characterized by having a structure comprising a bisphenol compound represented by the general formula (II) and a trisphenol represented by the general formula (III) in a positive photosensitive resin composition; The above-described semiconductor device using a positive photosensitive resin composition comprising a compound and a total of 1 to 30 parts by weight of both.

【0006】[0006]

【化6】 Embedded image

【0007】[0007]

【化7】 Embedded image

【0008】[0008]

【化8】 Embedded image

【0009】式(I)のポリアミドは、Xの構造を有す
るビスアミノフェノールとYの構造を有するジカルボン
酸と、更にEの構造を有する酸無水物からなり、このポ
リアミドを約300〜400℃で加熱すると脱水閉環
し、ポリベンゾオキサゾールという耐熱性樹脂に変化す
る。本発明のポリアミド(I)のXは、例えば、
The polyamide of the formula (I) comprises a bisaminophenol having the structure of X, a dicarboxylic acid having the structure of Y and an acid anhydride having the structure of E. When heated, the ring is dehydrated and closed, and changes to a heat-resistant resin called polybenzoxazole. X of the polyamide (I) of the present invention is, for example,

【0010】[0010]

【化9】 Embedded image

【0011】等であるがこれらに限定されるものではな
い。この中で特に好ましいものとしては、
However, the present invention is not limited to these. Among them, particularly preferred are:

【0012】[0012]

【化10】 Embedded image

【0013】より選ばれるものである。又式(I)のY
は、例えば、
[0013] It is more selected. In the formula (I), Y
Is, for example,

【0014】[0014]

【化11】 Embedded image

【0015】等であるがこれらに限定されるものではな
い。これらの中で特に好ましいものとしては、
However, the present invention is not limited to these. Particularly preferred among these are:

【0016】[0016]

【化12】 Embedded image

【0017】より選ばれるものである。又式(I)のE
は、例えば、
[0017] It is selected more. In addition, E of the formula (I)
Is, for example,

【0018】[0018]

【化13】 Embedded image

【0019】等が挙げられるが、これらに限定されるも
のではない。この中で特に好ましいものとしては、
However, the present invention is not limited to these. Among them, particularly preferred are:

【0020】[0020]

【化14】 Embedded image

【0021】より選ばれるものである。本発明はYの構
造を有するジカルボン酸誘導体とXの構造を有するビス
アミノフェノールを反応させてポリアミドを合成した
後、式(I)のEに示すアルケニル基又はアルキニル基
を少なくとも1個有する酸無水物を用いて末端のアミノ
基をキャップするものである。更に、式(I)のZは、
例えば
[0021] In the present invention, a polyamide is synthesized by reacting a dicarboxylic acid derivative having a structure of Y with a bisaminophenol having a structure of X, and then an acid anhydride having at least one alkenyl group or alkynyl group represented by E in the formula (I). The terminal amino group is capped with a substance. Further, Z in the formula (I) is
For example

【0022】[0022]

【化15】 Embedded image

【0023】等であるがこれらに限定されるものではな
い。式(1)のZは、例えば、シリコンウェハーのよう
な基板に対して、特に優れた密着性が必要な場合に用い
るが、その使用割合bは最大40.0モル%までであ
る。40.0モル%を越えると樹脂の溶解性が極めて低
下し、現像残り(スカム)が発生し、パターン加工がで
きない。なお、これらX、Y、E、Zの使用にあたって
は、それぞれ1種類であっても2種類以上の混合物であ
っても構わない。
However, the present invention is not limited to these. Z in the formula (1) is used, for example, when particularly excellent adhesion is required to a substrate such as a silicon wafer, and the use ratio b is up to 40.0 mol%. If it exceeds 40.0 mol%, the solubility of the resin is extremely reduced, and undeveloped portions (scum) are generated, and pattern processing cannot be performed. In using these X, Y, E, and Z, one type or a mixture of two or more types may be used.

【0024】本発明で用いる感光性ジアゾキノン化合物
は、1,2−ベンゾキノンジアジドあるいは1,2−ナ
フトキノンジアジド構造を有する化合物と、支持体であ
るフェノール系化合物との反応物である。
The photosensitive diazoquinone compound used in the present invention is a reaction product of a compound having a 1,2-benzoquinonediazide or 1,2-naphthoquinonediazide structure and a phenol compound as a support.

【0025】本発明のポジ型感光性樹脂組成物において
は、現像時に特に高感度、高残膜率を得る目的で、一般
式(II)又は一般式(III)で示される構造を有する感
光性ジアゾキノン化合物を組成に加えることが重要であ
る。ポジ型の感光性樹脂の現像メカニズムは前述したよ
うに露光部と未露光部との溶解性の差を利用しており、
高感度、高残膜率を得ようとする場合、その差を大きく
するために露光部はより溶けやすく、未露光部はより溶
けにくくなるように溶解性を変化させることが必要であ
る。その溶解性の差の変化は支持体であるフェノール系
化合物の構造にも因るところが大きい。そこで現像時に
おいて、露光部では溶解性を促進させ、かつ未露光部で
は溶解阻止効果を助けて十分な残膜率を保持させること
ができる支持体を有する感光性ジアゾキノン化合物を探
索した結果、下記の化合物が高感度を保ちながら高残膜
率を発現することを見いだした。感光性ジアゾキノン化
合物としては、下記のもの等が挙げられるがこれらに限
定されるものではない。
In the positive photosensitive resin composition of the present invention, a photosensitive resin having a structure represented by the general formula (II) or (III) for the purpose of obtaining particularly high sensitivity and a high residual film ratio during development. It is important to add a diazoquinone compound to the composition. The development mechanism of the positive photosensitive resin utilizes the difference in solubility between the exposed part and the unexposed part as described above.
In order to obtain a high sensitivity and a high residual film ratio, it is necessary to change the solubility so that the exposed portion becomes more soluble and the unexposed portion becomes less soluble in order to increase the difference. The change in the difference in solubility largely depends on the structure of the phenolic compound as the support. Therefore, at the time of development, a photosensitive diazoquinone compound having a support capable of promoting the solubility in the exposed portion and promoting the dissolution inhibiting effect in the unexposed portion and maintaining a sufficient remaining film ratio was searched for. Was found to exhibit a high residual film ratio while maintaining high sensitivity. Examples of the photosensitive diazoquinone compound include the following, but are not limited thereto.

【0026】[0026]

【化16】 Embedded image

【0027】[0027]

【化17】 Embedded image

【0028】また、感光性ジアゾキノン化合物のポリア
ミドへの配合量は、ポリアミド100重量部に対し、1
〜100重量部で、配合量が1重量部未満だと樹脂のパ
ターニング性が不良であり、逆に100重量部を越える
と感度が大幅に低下するだけでなく、フィルムの引張り
伸び率が著しく低下する。
The amount of the photosensitive diazoquinone compound in the polyamide is 1 to 100 parts by weight of the polyamide.
When the amount is less than 1 part by weight, the patterning property of the resin is poor. On the contrary, when the amount exceeds 100 parts by weight, not only the sensitivity is significantly reduced, but also the tensile elongation of the film is significantly reduced. I do.

【0029】本発明のポジ型感光性樹脂組成物には、必
要により感光特性を高めるためにジヒドロピリジン誘導
体を加えることができる。ジヒドロピリジン誘導体とし
ては、例えば2,6−ジメチル−3,5−ジアセチル−
4−(2′−ニトロフェニル)−1,4−ジヒドロピリ
ジン、4−(2′−ニトロフェニル)−2,6−ジメチ
ル−3,5−ジカルボエトキシ−1,4−ジヒドロピリ
ジン、4−(2′,4′−ジニトロフェニル)−2,6
−ジメチル−3,5−ジカルボメトキシ−1,4−ジヒ
ドロピリジン等を挙げることができる。
A dihydropyridine derivative can be added to the positive photosensitive resin composition of the present invention, if necessary, to enhance the photosensitive characteristics. Examples of the dihydropyridine derivative include 2,6-dimethyl-3,5-diacetyl-
4- (2'-nitrophenyl) -1,4-dihydropyridine, 4- (2'-nitrophenyl) -2,6-dimethyl-3,5-dicarbethoxy-1,4-dihydropyridine, 4- (2 ', 4'-Dinitrophenyl) -2,6
-Dimethyl-3,5-dicarbomethoxy-1,4-dihydropyridine and the like.

【0030】本発明のポジ型感光性樹脂組成物において
は更に一般式(II)で示されるビスフェノール化合物と
一般式(III)で示されるトリスフェノール化合物とを
併用することが重要である。これら一般式(II)、一般
式(III)で示されるフェノール化合物類をポリベンゾ
オキサゾール前駆体とジアゾキノン化合物より構成され
るポジ型感光性樹脂組成に加えると封止樹脂との密着性
が向上し、更に現像時において高感度、高残膜率が得ら
れ、また、−60〜−50℃の低温で保管しても、フェ
ノールの析出等が無く保存性に優れたポジ型感光性樹脂
組成物が得られる。封止樹脂との密着性は一般式(I
I)、一般式(III)で示されるフェノール化合物類を単
独で加えるだけでもある程度は有効であるが、それぞれ
単独で添加量を増やすと、一般式(II)で示されるビス
フェノール化合物は、−60〜−50℃の低温で保管す
ると、析出が起こりやすくなる。また一般式(III)で
示されるトリスフェノール化合物は、著しい残膜率の低
下が見られる。しかし一般式(II)で示されるビスフェ
ノール化合物と一般式(III)で示されるトリスフェノ
ール化合物とを併用することにより、各々が有する欠点
が改善され、更に高感度の感光特性と封止樹脂との優れ
た密着性も発現した。
In the positive photosensitive resin composition of the present invention, it is further important to use a bisphenol compound represented by the general formula (II) in combination with a trisphenol compound represented by the general formula (III). When these phenolic compounds represented by the general formulas (II) and (III) are added to a positive photosensitive resin composition composed of a polybenzoxazole precursor and a diazoquinone compound, the adhesion to a sealing resin is improved. Further, a positive photosensitive resin composition which has a high sensitivity and a high residual film ratio at the time of development, and has excellent preservability without phenol precipitation or the like even when stored at a low temperature of -60 to -50 ° C. Is obtained. The adhesion to the sealing resin is determined by the general formula (I
It is effective to some extent to add only the phenolic compounds represented by I) and general formula (III) to a certain extent. However, when the addition amount of each compound alone is increased, the bisphenol compound represented by general formula (II) becomes −60 When stored at a low temperature of -50C, precipitation tends to occur. Further, the trisphenol compound represented by the general formula (III) has a remarkable decrease in the residual film ratio. However, by using the bisphenol compound represented by the general formula (II) and the trisphenol compound represented by the general formula (III) in combination, the disadvantages of each compound can be improved, and the photosensitivity of high sensitivity and the sealing resin can be improved. Excellent adhesion was also exhibited.

【0031】フェノール化合物類の添加量は、一般式
(I)で示されるポリアミド100重量部に対して、一
般式(II)で表わされるビスフェノール化合物と一般式
(III)で表わされるトリスフェノール化合物を両者合
計1〜30重量部である。両フェノール化合物の添加量
が30重量部より多いと、前述のように−60〜−50
℃の低温保管で析出が生じたり、現像時に著しい残膜率
の低下が起こる。添加量が1重量部未満では、封止樹脂
との密着性が低下するばかりか現像時における感度が低
下する。一般式(II)に示されるビスフェノール化合物
としては下記のもの等を挙げることができるがこれらに
限定されない。
The amount of the phenol compound added is such that the bisphenol compound represented by the general formula (II) and the trisphenol compound represented by the general formula (III) are added to 100 parts by weight of the polyamide represented by the general formula (I). The total amount is 1 to 30 parts by weight. When the addition amount of both phenol compounds is more than 30 parts by weight, -60 to -50 as described above.
Precipitation occurs during storage at a low temperature of ℃, and a significant decrease in the residual film ratio occurs during development. When the addition amount is less than 1 part by weight, not only the adhesion to the sealing resin is lowered but also the sensitivity at the time of development is lowered. Examples of the bisphenol compound represented by the general formula (II) include, but are not limited to, the following.

【0032】[0032]

【化18】 Embedded image

【0033】[0033]

【化19】 Embedded image

【0034】[0034]

【化20】 Embedded image

【0035】[0035]

【化21】 Embedded image

【0036】これらの中で特に、好ましいものとして
は、
Of these, particularly preferred are:

【0037】[0037]

【化22】 Embedded image

【0038】である。また、一般式(III)に示される
化合物としては下記のもの等を挙げることができるがこ
れらに限定されない。
Is as follows. In addition, examples of the compound represented by the general formula (III) include the following, but are not limited thereto.

【0039】[0039]

【化23】 Embedded image

【0040】[0040]

【化24】 Embedded image

【0041】[0041]

【化25】 Embedded image

【0042】これらの中で特に、好ましいものとして
は、
Of these, particularly preferred are:

【0043】[0043]

【化26】 Embedded image

【0044】である。本発明におけるポジ型感光性樹脂
組成物には、必要によりレベリング剤、シランカップリ
ング剤等の添加剤を添加することができる。本発明にお
いてはこれらの成分を溶剤に溶解し、ワニス状にして使
用する。溶剤としては、N−メチル−2−ピロリドン、
γ−ブチロラクトン、N,N−ジメチルアセトアミド、
ジメチルスルホキシド、ジエチレングリコールジメチル
エーテル、ジエチレングリコールジエチルエーテル、ジ
エチレングリコールジブチルエーテル、プロピレングリ
コールモノメチルエーテル、ジプロピレングリコールモ
ノメチルエーテル、プロピレングリコールモノメチルエ
ーテルアセテート、乳酸メチル、乳酸エチル、乳酸ブチ
ル、メチル−1,3−ブチレングリコールアセテート、
1,3−ブチレングリコール−3−モノメチルエーテ
ル、ピルビン酸メチル、ピルビン酸エチル、メチル−3
−メトキシプロピオネート等が挙げられ、単独でも混合
して用いてもよい。
Is as follows. If necessary, additives such as a leveling agent and a silane coupling agent can be added to the positive photosensitive resin composition of the present invention. In the present invention, these components are dissolved in a solvent and used in the form of a varnish. As the solvent, N-methyl-2-pyrrolidone,
γ-butyrolactone, N, N-dimethylacetamide,
Dimethyl sulfoxide, diethylene glycol dimethyl ether, diethylene glycol diethyl ether, diethylene glycol dibutyl ether, propylene glycol monomethyl ether, dipropylene glycol monomethyl ether, propylene glycol monomethyl ether acetate, methyl lactate, ethyl lactate, butyl lactate, methyl-1,3-butylene glycol acetate,
1,3-butylene glycol-3-monomethyl ether, methyl pyruvate, ethyl pyruvate, methyl-3
-Methoxypropionate, etc., which may be used alone or as a mixture.

【0045】本発明のポジ型感光性樹脂組成物の使用方
法は、まず該組成物を適当な支持体、例えば、シリコン
ウェハー、セラミック基板、アルミ基板等に塗布する。
塗布量は、半導体装置の場合、硬化後の最終膜厚が0.
1〜20μmになるよう塗布する。膜厚が0.1μm以
下であると、半導体素子の保護表面膜としての機能を十
分に発揮することが困難となり、20μm以上である
と、微細な加工パターンを得ることが困難となるばかり
でなく、加工に時間がかかりスループットが低下する。
塗布方法としては、スピンナーを用いた回転塗布、スプ
レーコーターを用いた噴霧塗布、浸漬、印刷、ロールコ
ーティング等がある。次に、60〜130℃でプリベー
クして塗膜を乾燥後、所望のパターン形状に化学線を照
射する。化学線としては、X線、電子線、紫外線、可視
光線等が使用できるが、200〜500nmの波長のも
のが好ましい。次に照射部を現像液で溶解除去すること
によりレリーフパターンを得る。現像液としては、水酸
化ナトリウム、水酸化カリウム、炭酸ナトリウム、ケイ
酸ナトリウム、メタケイ酸ナトリウム、アンモニア水等
の無機アルカリ類、エチルアミン、n−プロピルアミン
等の第1アミン類、ジエチルアミン、ジ−n−プロピル
アミン等の第2アミン類、トリエチルアミン、メチルジ
エチルアミン等の第3アミン類、ジメチルエタノールア
ミン、トリエタノールアミン等のアルコールアミン類、
テトラメチルアンモニウムヒドロキシド、テトラエチル
アンモニウムヒドロキシド等の第4級アンモニウム塩等
のアルカリ類の水溶液、及びこれにメタノール、エタノ
ールのごときアルコール類等の水溶性有機溶媒や界面活
性剤を適当量添加した水溶液を好適に使用することがで
きる。現像方法としては、スプレー、パドル、浸漬、超
音波等の方式が可能である。次に、現像によって形成し
たレリーフパターンをリンスする。リンス液としては、
蒸留水を使用する。次に加熱処理を行い、オキサゾール
環を形成し、耐熱性に富む最終パターンを得る。
In the method of using the positive photosensitive resin composition of the present invention, the composition is first applied to a suitable support, for example, a silicon wafer, a ceramic substrate, an aluminum substrate or the like.
In the case of a semiconductor device, the amount of coating is 0.1 μm for the final film thickness after curing.
It is applied so as to have a thickness of 1 to 20 μm. When the thickness is 0.1 μm or less, it is difficult to sufficiently exert the function as a protective surface film of the semiconductor element, and when it is 20 μm or more, it becomes difficult to obtain a fine processing pattern, In addition, processing takes time and the throughput is reduced.
Examples of the coating method include spin coating using a spinner, spray coating using a spray coater, dipping, printing, and roll coating. Next, after pre-baking at 60 to 130 ° C. to dry the coating film, a desired pattern shape is irradiated with actinic radiation. As the actinic radiation, X-rays, electron beams, ultraviolet rays, visible rays and the like can be used, but those having a wavelength of 200 to 500 nm are preferable. Next, a relief pattern is obtained by dissolving and removing the irradiated portion with a developer. Examples of the developer include inorganic alkalis such as sodium hydroxide, potassium hydroxide, sodium carbonate, sodium silicate, sodium metasilicate, and aqueous ammonia, primary amines such as ethylamine and n-propylamine, diethylamine, and di-n. Secondary amines such as propylamine, tertiary amines such as triethylamine and methyldiethylamine, alcoholamines such as dimethylethanolamine and triethanolamine,
An aqueous solution of an alkali such as a quaternary ammonium salt such as tetramethylammonium hydroxide or tetraethylammonium hydroxide, and an aqueous solution obtained by adding an appropriate amount of a water-soluble organic solvent such as alcohol such as methanol or ethanol or a surfactant. Can be suitably used. As a developing method, a system such as spray, paddle, immersion, and ultrasonic wave can be used. Next, the relief pattern formed by development is rinsed. As the rinse liquid,
Use distilled water. Next, heat treatment is performed to form an oxazole ring, and a final pattern having high heat resistance is obtained.

【0046】次に、本発明の感光性樹脂組成物を用いた
LOC型構造を有する半導体装置への応用例について図
面を用いて説明する。図1は、本発明のLOC型構造を
有する樹脂封止型半導体装置の断面図で、チップ2上に
本発明の感光性樹脂組成物のコート層があり、パターニ
ング、硬化後、このコート層を接着剤1としてチップ2
とリードフレーム3を接着固定し、チップ2とリードフ
レーム3を金線ワイヤ4で接続した後、樹脂封止5で封
止したものである。接着方法としては、チップを200
〜450℃に加熱し、0.1〜10Kg/cm2の圧力
で数秒間圧着する。図2は、従来のLOC型構造を有す
る樹脂封止型半導体装置の断面図で接着剤1'付き絶縁
フィルム6を介してチップ2とリードフレーム3を接着
固定した後、封止樹脂5で封止したものである。従来は
接着剤1'付き絶縁フィルム6をリードフレーム3に接
着した後、チップ2とリードフレーム3を接着するので
作業性がよくない。接着剤1'付き絶縁フィルム6の絶
縁フィルムとしては、吸水率、線膨張係数の大きな20
μm程度のポリイミドフィルムを用いているので、半田
浸せき時にパッケージクラックが発生するという問題が
あったが、本発明の感光性樹脂の接着層は低吸水率で薄
膜のためパッケージクラックの発生がなく、高信頼性の
LOC構造を有する樹脂封止型半導体装置が得られる。
Next, an example of application to a semiconductor device having a LOC structure using the photosensitive resin composition of the present invention will be described with reference to the drawings. FIG. 1 is a cross-sectional view of a resin-encapsulated semiconductor device having a LOC structure according to the present invention. A chip 2 has a coating layer of a photosensitive resin composition of the present invention. Chip 2 as adhesive 1
And the lead frame 3 are bonded and fixed, the chip 2 and the lead frame 3 are connected with the gold wire 4, and then sealed with the resin sealing 5. As the bonding method, the chip is 200
Heat to 450450 ° C. and crimp for several seconds at a pressure of 0.1 to 10 kg / cm 2 . FIG. 2 is a cross-sectional view of a conventional resin-encapsulated semiconductor device having a LOC type structure. The chip 2 and the lead frame 3 are bonded and fixed via an insulating film 6 with an adhesive 1 ′, and then sealed with a sealing resin 5. It is stopped. Conventionally, since the chip 2 and the lead frame 3 are bonded after bonding the insulating film 6 with the adhesive 1 'to the lead frame 3, workability is not good. As the insulating film of the insulating film 6 with the adhesive 1 ', a water absorbing coefficient and a linear expansion coefficient of 20
Since a polyimide film of about μm was used, there was a problem that package cracks occurred during solder immersion, but the adhesive layer of the photosensitive resin of the present invention did not cause package cracks due to a thin film with a low water absorption, A resin-encapsulated semiconductor device having a highly reliable LOC structure can be obtained.

【0047】[0047]

【実施例】以下、実施例により本発明を具体的に説明す
る。 《実施例1》 *ポリアミドの合成 ジフェニルエーテル−4,4’−ジカルボン酸1モルと
1−ヒドロキシ−1,2,3−ベンゾトリアゾール2モ
ルとを反応させて得られたジカルボン酸誘導体443.
2g(0.9モル)とヘキサフルオロ−2,2−ビス
(3−アミノ−4−ヒドロキシフェニル)プロパン36
6.3g(1.0モル)とを温度計、攪拌機、原料投入
口、乾燥窒素ガス導入管を備えた4つ口のセパラブルフ
ラスコに入れ、N−メチル−2−ピロリドン3000g
を加えて溶解させた。その後オイルバスを用いて75℃
にて12時間反応させた。次にN−メチル−2−ピロリ
ドン500gに溶解させた5−ノルボルネン−2,3−
ジカルボン酸無水物32.8g(0.2モル)を加え、
更に12時間攪拌して反応を終了した。反応混合物をろ
過した後、反応混合物を水/メタノール=3/1の溶液
に投入、沈殿物を濾集し水で充分洗浄した後、真空下で
乾燥し、目的のポリアミド(A−1)を得た。
The present invention will be described below in detail with reference to examples. << Example 1 >> * Synthesis of polyamide Dicarboxylic acid derivative 443. obtained by reacting 1 mol of diphenyl ether-4,4'-dicarboxylic acid with 2 mol of 1-hydroxy-1,2,3-benzotriazole.
2 g (0.9 mol) and hexafluoro-2,2-bis (3-amino-4-hydroxyphenyl) propane 36
6.3 g (1.0 mol) were put into a four-neck separable flask equipped with a thermometer, a stirrer, a raw material inlet, and a dry nitrogen gas inlet tube, and 3000 g of N-methyl-2-pyrrolidone was added.
And dissolved. Then use an oil bath at 75 ° C
For 12 hours. Next, 5-norbornene-2,3- dissolved in 500 g of N-methyl-2-pyrrolidone.
32.8 g (0.2 mol) of dicarboxylic anhydride were added,
The reaction was further stirred for 12 hours to complete the reaction. After filtering the reaction mixture, the reaction mixture was poured into a solution of water / methanol = 3/1, the precipitate was collected by filtration, washed sufficiently with water, and dried under vacuum to obtain the desired polyamide (A-1). Obtained.

【0048】*ポジ型感光性樹脂組成物の作製 合成したポリアミド(A−1)100g、下記式の構造
を有するジアゾキノン(B−1)25gをN−メチル−
2−ピロリドン250gに溶解した後、0.2μmのテ
フロンフィルターで濾過し感光性樹脂組成物を得た。
* Preparation of Positive Photosensitive Resin Composition 100 g of the synthesized polyamide (A-1) and 25 g of diazoquinone (B-1) having a structure of the following formula were added to N-methyl-
After dissolving in 250 g of 2-pyrrolidone, the solution was filtered through a 0.2 μm Teflon filter to obtain a photosensitive resin composition.

【0049】*特性評価 このポジ型感光性樹脂組成物をシリコンウェハー上にス
ピンコーターを用いて塗布した後、ホットプレートにて
120℃で4分乾燥し、膜厚約5μmの塗膜を得た。こ
の塗膜にg線ステッパー露光機NSR−1505G3A
(ニコン(株)製)によりレチクルを通して50mJ/c
2から10mJ/cm2ずつ増やして540mJ/cm
2まで露光を行った。次に1.40%のテトラメチルア
ンモニウムヒドロキシド水溶液に60秒浸漬することに
よって露光部を溶解除去した後、純水で30秒間リンス
した。その結果、露光量230mJ/cm2で照射した
部分よりパターンが成形されていることが確認できた。
(感度は230mJ/cm2)。この時の残膜率(現像
後の膜厚/現像前の膜厚×100)は93.1%と非常
に高い値を示した。また、吸水率は0.3%であった。
次に前記シリコンウエハを6×15mmにダイシング
し、得られた半導体チップを42合金製リードフレーム
に400℃で1秒加圧(1Kg/cm2)接着した。そ
の後エポキシ樹脂系封止材料でLOC構造の300mi
l幅のSOJに封止した。この封止品20個を85℃/
85%RH下に16時間放置した後、IRフロー(24
0℃×10秒)にかけ、パッケージにクラックが発生す
る数を調べたところ、クラック発生数は0/20であっ
た。
* Characteristic evaluation After applying this positive photosensitive resin composition on a silicon wafer using a spin coater, it was dried on a hot plate at 120 ° C. for 4 minutes to obtain a coating film having a thickness of about 5 μm. . G-line stepper exposure machine NSR-1505G3A
50 mJ / c through a reticle by Nikon Corporation
Increase from m 2 by 10mJ / cm 2 540mJ / cm
Exposure was performed up to 2 . Next, the exposed portion was dissolved and removed by immersion in a 1.40% aqueous solution of tetramethylammonium hydroxide for 60 seconds, and then rinsed with pure water for 30 seconds. As a result, it was confirmed that a pattern was formed from a portion irradiated with an exposure amount of 230 mJ / cm 2 .
(The sensitivity is 230 mJ / cm 2 ). At this time, the residual film ratio (film thickness after development / film thickness before development × 100) showed a very high value of 93.1%. The water absorption was 0.3%.
Next, the silicon wafer was diced into 6 × 15 mm, and the obtained semiconductor chip was bonded to a 42 alloy lead frame at 400 ° C. for 1 second (1 kg / cm 2 ). After that, 300mi of LOC structure with epoxy resin type sealing material
It was sealed in an SOJ having a width of l. 85 of this sealed product
After standing at 85% RH for 16 hours, the IR flow (24
(0 ° C. × 10 seconds), and the number of cracks generated in the package was examined. The number of cracks generated was 0/20.

【0050】《実施例2》実施例1におけるポリアミド
の合成において、ジフェニルエーテル−4,4’−ジカ
ルボン酸1モルと1−ヒドロキシ−1,2,3−ベンゾ
トリアゾール2モルとを反応させて得られたジカルボン
酸誘導体の代わりに、アジンピン酸1モルと1−ヒドロ
キシ−1,2,3−ベンゾトリアゾール2モルとを反応
させて得られたジカルボン酸誘導体を用いてポリアミド
(A−2)を合成し、その他は実施例1と同様の評価を
行った。
Example 2 In the synthesis of the polyamide in Example 1, it was obtained by reacting 1 mol of diphenyl ether-4,4'-dicarboxylic acid with 2 mol of 1-hydroxy-1,2,3-benzotriazole. A polyamide (A-2) was synthesized using a dicarboxylic acid derivative obtained by reacting 1 mol of azine pinic acid with 2 mol of 1-hydroxy-1,2,3-benzotriazole instead of the dicarboxylic acid derivative obtained above. The other evaluations were the same as in Example 1.

【0051】《実施例3》実施例1におけるポリアミド
の合成においてヘキサフルオロ−2,2−ビス(3−ア
ミノ−4−ヒドロキシフェニル)プロパンの替わりに
3,3’−ジアミノ−4,4’−ジヒドロキシジフェニ
ルスルホンを用いて、ポリアミド(A−3)を合成し、
その他は実施例1と同様の評価を行った。
Example 3 In the synthesis of the polyamide in Example 1, instead of hexafluoro-2,2-bis (3-amino-4-hydroxyphenyl) propane, 3,3'-diamino-4,4'- Polyamide (A-3) is synthesized using dihydroxydiphenyl sulfone,
Otherwise, the same evaluation as in Example 1 was performed.

【0052】《実施例4》実施例1におけるポリアミド
の合成において5−ノルボルネン−2,3−ジカルボン
酸無水物の替わりに無水マレイン酸を用いてポリアミド
(A−4)を合成し、その他は実施例1と同様の評価を
行った。
Example 4 In the synthesis of a polyamide in Example 1, a polyamide (A-4) was synthesized using maleic anhydride instead of 5-norbornene-2,3-dicarboxylic anhydride, and the other steps were performed. The same evaluation as in Example 1 was performed.

【0053】《実施例5》実施例1における感光性樹脂
組成物中の感光性ジアゾキノン化合物B−1をB−2に
替えて、更に該成分の添加量を表1の様に替えた他は実
施例1と同様の評価を行った。
Example 5 The procedure of Example 1 was repeated except that the photosensitive diazoquinone compound B-1 in the photosensitive resin composition was changed to B-2 and the amount of the component was changed as shown in Table 1. The same evaluation as in Example 1 was performed.

【0054】《実施例6》実施例1における感光性樹脂
組成物中の感光性ジアゾキノン化合物B−1をB−3に
替えて、更に該成分の添加量を表1の様に替えた他は実
施例1と同様の評価を行った。
Example 6 The procedure of Example 1 was repeated except that the photosensitive diazoquinone compound B-1 in the photosensitive resin composition was changed to B-3 and the amount of the component was changed as shown in Table 1. The same evaluation as in Example 1 was performed.

【0055】《実施例7》実施例1における感光性樹脂
組成物中の感光性ジアゾキノン化合物B−1の添加量を
表1の様に替えた他は実施例1と同様の評価を行った。
Example 7 The same evaluation as in Example 1 was performed except that the amount of the photosensitive diazoquinone compound B-1 in the photosensitive resin composition in Example 1 was changed as shown in Table 1.

【0056】《実施例8》実施例1における感光性樹脂
組成物中にビスフェノール化合物C−1 10gを添加
した他は実施例1と同様の評価を行った。
Example 8 The same evaluation as in Example 1 was performed except that 10 g of bisphenol compound C-1 was added to the photosensitive resin composition in Example 1.

【0057】《比較例1》カプトンフィルム(吸水率2
%)の両面にポリエーテルアミド系の接着剤が塗布され
ている絶縁フィルムを用いて、実施例1と同様に半導体
チップと42合金製リードフレームを400℃、1秒で
加圧(1Kg/cm2)接着し、エポキシ樹脂系封止材
料で封止した。この半導体装置のパッケージクラックを
調べたところ15/20であった。
Comparative Example 1 Kapton film (water absorption 2
%), The semiconductor chip and the 42 alloy lead frame were pressed at 400 ° C. for 1 second (1 kg / cm) using an insulating film having both surfaces coated with a polyetheramide-based adhesive in the same manner as in Example 1. 2 ) Bonded and sealed with epoxy resin sealing material. When the package crack of this semiconductor device was examined, it was 15/20.

【0058】《比較例2》ユーピレックスフィルム(吸
水率1%)に比較例1と同様の接着剤を塗布し、実施例
1と同様にして半導体装置を作製した。この半導体装置
のパッケージクラックを調べたところ9/20であっ
た。
Comparative Example 2 An adhesive similar to that of Comparative Example 1 was applied to an Iupirex film (water absorption: 1%), and a semiconductor device was fabricated in the same manner as in Example 1. When the package crack of this semiconductor device was examined, it was 9/20.

【0059】[0059]

【表1】 [Table 1]

【0060】[0060]

【化27】 Embedded image

【0061】[0061]

【化28】 Embedded image

【0062】[0062]

【発明の効果】本発明によれば、チップとリードフレー
ムの接着が従来技術に比べ、大幅な作業工数の短縮が可
能になる。またリフロー時に前記絶縁フィルム中に吸水
された水分がパッケージの中で気化膨張するのを低減す
ることができるのでパッケージクラックの発生を防止で
きる。従って、安価で高信頼性のLOC構造の樹脂封止
型半導体装置を提供できる。
According to the present invention, the bonding between the chip and the lead frame can be greatly reduced as compared with the prior art. In addition, it is possible to prevent the moisture absorbed in the insulating film from evaporating and expanding in the package during the reflow, so that the occurrence of a package crack can be prevented. Therefore, an inexpensive and highly reliable resin-encapsulated semiconductor device having a LOC structure can be provided.

【図面の簡単な説明】[Brief description of the drawings]

【図1】図1は本発明のLOC構造を有する樹脂封止型
半導体装置の断面図である。
FIG. 1 is a cross-sectional view of a resin-sealed semiconductor device having a LOC structure according to the present invention.

【図2】図2は従来技術によるLOC構造を有する樹脂
封止型半導体装置の断面図である。
FIG. 2 is a cross-sectional view of a resin-sealed semiconductor device having a LOC structure according to the related art.

【符号の説明】[Explanation of symbols]

1 接着剤 1' 接着剤 2 チップ 3 リードフレーム 4 金線ワイヤ 5 封止樹脂 6 絶縁フィルム DESCRIPTION OF SYMBOLS 1 Adhesive 1 'Adhesive 2 Chip 3 Lead frame 4 Gold wire 5 Sealing resin 6 Insulating film

フロントページの続き Fターム(参考) 2H025 AA01 AA14 AB16 AB17 AC01 AD03 BE01 CB25 CB32 CB45 CC06 CC20 4J001 DA01 DB03 DC04 DC08 DC10 DC14 DD02 EB34 EB57 EB58 EB60 EC66 EC67 EC70 EC79 EE22C EE27C GE01 JA07 JA18 JB18 JB34 JB45 4J040 EG021 GA29 HB21 HC14 MA02 NA20 5F047 AA11 BA24 BA35 BA39 BB11 BB16 BB19 Continued on the front page F-term (reference) 2H025 AA01 AA14 AB16 AB17 AC01 AD03 BE01 CB25 CB32 CB45 CC06 CC20 4J001 DA01 DB03 DC04 DC08 DC10 DC14 DD02 EB34 EB57 EB58 EB60 EC66 EC67 EC70 EC79 EE22C EE27C GE01 J07J18J18 J18 J18B18 J18 HC14 MA02 NA20 5F047 AA11 BA24 BA35 BA39 BB11 BB16 BB19

Claims (4)

【特許請求の範囲】[Claims] 【請求項1】 一般式(I)で示されるポリアミド10
0重量部と感光性ジアゾキノン化合物1〜100重量部
とからなるポジ型感光性樹脂組成物のコート層を半導体
チップの回路素子形成面上に有し、該コート層を接着剤
とし、複数のインナーリードを前記半導体チップと接着
し、該インナーリードと半導体チップとが、ボンディン
グワイヤで接続され、封止樹脂で封止されたリードオン
チップ(Lead On Chip)構造を有すること
を特徴とする樹脂封止型半導体装置。 【化1】
1. Polyamide 10 represented by the general formula (I)
A coating layer of a positive photosensitive resin composition comprising 0 parts by weight and a photosensitive diazoquinone compound in an amount of from 1 to 100 parts by weight on a circuit element forming surface of a semiconductor chip; A resin seal having a lead-on-chip (Lead On Chip) structure in which a lead is bonded to the semiconductor chip, and the inner lead and the semiconductor chip are connected by a bonding wire and sealed with a sealing resin. Stop type semiconductor device. Embedded image
【請求項2】 請求項1記載のポジ型感光性樹脂組成物
が、さらに一般式(II)で表わされるビスフェノール化
合物および一般式(III)で表わされるトリスフェノー
ル化合物を、両者合計1〜30重量部配合してなるポジ
型感光性樹脂組成物である請求項1記載の樹脂封止型半
導体装置。 【化2】 【化3】
2. The positive photosensitive resin composition according to claim 1, further comprising a bisphenol compound represented by the general formula (II) and a trisphenol compound represented by the general formula (III) in a total of 1 to 30% by weight. The resin-encapsulated semiconductor device according to claim 1, wherein the resin-encapsulated semiconductor device is a positive photosensitive resin composition obtained by mixing parts. Embedded image Embedded image
【請求項3】 請求項1記載のポジ型感光性樹脂組成物
の一般式(I)のポリアミドにおけるXが、下記より選
ばれてなる請求項1又は2記載の樹脂封止型半導体装
置。 【化4】
3. The resin-encapsulated semiconductor device according to claim 1, wherein X in the polyamide of the general formula (I) of the positive photosensitive resin composition according to claim 1 is selected from the following. Embedded image
【請求項4】 請求項1記載のポジ型感光性樹脂組成物
の一般式(I)のポリアミドにおけるYが、下記より選
ばれてなる請求項1、2又は3記載の樹脂封止型半導体
装置。 【化5】
4. The resin-encapsulated semiconductor device according to claim 1, wherein Y in the polyamide of the general formula (I) of the positive photosensitive resin composition according to claim 1 is selected from the following. . Embedded image
JP33355398A 1998-11-25 1998-11-25 Resin-sealed semiconductor device Expired - Fee Related JP3313331B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP33355398A JP3313331B2 (en) 1998-11-25 1998-11-25 Resin-sealed semiconductor device

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP33355398A JP3313331B2 (en) 1998-11-25 1998-11-25 Resin-sealed semiconductor device

Publications (2)

Publication Number Publication Date
JP2000164608A true JP2000164608A (en) 2000-06-16
JP3313331B2 JP3313331B2 (en) 2002-08-12

Family

ID=18267337

Family Applications (1)

Application Number Title Priority Date Filing Date
JP33355398A Expired - Fee Related JP3313331B2 (en) 1998-11-25 1998-11-25 Resin-sealed semiconductor device

Country Status (1)

Country Link
JP (1) JP3313331B2 (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2006096812A (en) * 2004-09-28 2006-04-13 Sumitomo Bakelite Co Ltd Resin composition for semiconductor surface protection film and semiconductor device produced by using the same
WO2007004345A1 (en) * 2005-06-30 2007-01-11 Toray Industries, Inc. Photosensitive resin composition and adhesion enhancer
JP2009141016A (en) * 2007-12-04 2009-06-25 Hitachi Chem Co Ltd Method of manufacturing semiconductor device, photosensitive adhesive, and semiconductor device
JP2009278066A (en) * 2008-04-17 2009-11-26 Hitachi Chem Co Ltd Adhesive member for semiconductor, semiconductor device and method for manufacturing semiconductor device

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2006096812A (en) * 2004-09-28 2006-04-13 Sumitomo Bakelite Co Ltd Resin composition for semiconductor surface protection film and semiconductor device produced by using the same
WO2007004345A1 (en) * 2005-06-30 2007-01-11 Toray Industries, Inc. Photosensitive resin composition and adhesion enhancer
US7977028B2 (en) 2005-06-30 2011-07-12 Toray Industries, Inc. Photosensitive resin composition and adhesion promoter
JP2009141016A (en) * 2007-12-04 2009-06-25 Hitachi Chem Co Ltd Method of manufacturing semiconductor device, photosensitive adhesive, and semiconductor device
JP2009278066A (en) * 2008-04-17 2009-11-26 Hitachi Chem Co Ltd Adhesive member for semiconductor, semiconductor device and method for manufacturing semiconductor device

Also Published As

Publication number Publication date
JP3313331B2 (en) 2002-08-12

Similar Documents

Publication Publication Date Title
JP3207352B2 (en) Positive photosensitive resin composition
JP3958011B2 (en) Positive photosensitive resin composition, method for producing positive photosensitive resin composition, and semiconductor device
JP3667184B2 (en) Semiconductor device
JP4661245B2 (en) Positive photosensitive resin composition, semiconductor device and display element using the positive photosensitive resin composition, and manufacturing method of semiconductor device and display element
JP3478376B2 (en) Positive photosensitive resin composition
JP3919147B2 (en) Positive photosensitive resin composition and semiconductor device using the same
JP3176795B2 (en) Positive photosensitive resin composition
JP3449925B2 (en) Positive photosensitive resin composition
JP3313331B2 (en) Resin-sealed semiconductor device
JP3992351B2 (en) Positive photosensitive resin composition and semiconductor device using the same
JP4040216B2 (en) Positive photosensitive resin composition and semiconductor device using the same
JP3682898B2 (en) Positive photosensitive resin composition
JP3449926B2 (en) Positive photosensitive resin composition
JPH11102069A (en) Positive photosensitive resin composition
JP2002278051A (en) Positive type photosensitive resin composition and semiconductor device
JP3432437B2 (en) Developing solution for positive photosensitive resin composition and pattern forming method using the same
JP2000131845A (en) Positive photosensitive resin composition and semiconductor device made by using the same
JP3449931B2 (en) Positive photosensitive resin composition
JP3176802B2 (en) Positive photosensitive resin composition
JP3449933B2 (en) Positive photosensitive resin composition and semiconductor device using the same
JP3346981B2 (en) Semiconductor device
JP3449856B2 (en) Positive photosensitive resin composition
JP4197213B2 (en) Positive photosensitive resin composition and semiconductor device using the same
JP2002241611A (en) Positive type photo-sensitive resin composition and semiconductor device
JP4332958B2 (en) Method for processing positive photosensitive resin composition and semiconductor device

Legal Events

Date Code Title Description
FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20080531

Year of fee payment: 6

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20090531

Year of fee payment: 7

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20100531

Year of fee payment: 8

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20110531

Year of fee payment: 9

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20120531

Year of fee payment: 10

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20130531

Year of fee payment: 11

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20130531

Year of fee payment: 11

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20140531

Year of fee payment: 12

LAPS Cancellation because of no payment of annual fees